Title of Invention

“STEVIOL GLYCOSIDE ISOMERS”

Abstract

Steviol glycoside isomers are provided having the formula (II): wherein R1 may be hydrogen, 1-ß-D-glucopyranosyl, or 2-(1-ß-D-glucopyranosyl)-1-ß-D- glucopyranosyl, and R2 may be hydrogen, 1-ß-D-glucopyranosyl, 2-(1-ß-D-glucopyranosyl)- 1-ß-D-glucopyranosyl, 2,3 -bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L- rhamnopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-3 -(1-ß-D- glucopyranosyl)-1-ß-D-glucopyranosyl, or 2-(1-ß-D-xylopyranosyl)-3 -(1-ß-D- glucopyranosyl)-1-ß-D-glucopyranosyl. Methods for making steviol glycoside isomers are also disclosed. These compounds may be present in food and beverage products as non- nutritive sweeteners.

Full Text

STEVIOL GLYCOSIDE ISOMERS PRIORITY CLAIM [01] This application claims priority to PCT/US2008/075192, filed September 4, 2008 and entitled, Steviol Glycoside Isomers (Attorney Docket No. 056943.00325), which claims priority to U.S. Utility Patent Application Serial No. 11/856,274, filed September 17, 2007 and entitled, Steviol Glycoside Isomers (Attorney Docket No. 056943.00381), the entire disclosure of which is hereby incorporated by reference. FIELD OF THE INVENTION [02] This invention relates to certain novel isomers of steviol glycosides which are suitable for use as sweeteners, for example, by incorporation into food and beverage products. BACKGROUND [03] Due to increasing attention to the negative health effects of obesity in the United States and around the world, market demand for food and beverage products having alternative nutritional characteristics, including, for example, reduced or zero calorie content, has increased as well. There is market demand to replace the high-calorie sweeteners typically used in food and beverage products, such as sucrose and high fructose corn syrup (HFCS), with non-nutritive sweeteners. For example, diet cola beverages have been suggested which are sweetened with potent non-nutritive sweeteners such as steviol glycosides (stevioside, rebaudioside A, etc.). [04] Steviol glycosides are sweet-tasting compounds extracted from the stevia plant (Stevia rebaudiana Bertoni). Typically, these compounds are found to include stevioside (4-13% dry weight), steviolbioside (trace), the rebaudiosides, including rebaudioside A (1-6%), rebaudioside B (trace), rebaudioside C (1-2%), rebaudioside D (trace), and rebaudioside E (trace), and dulcoside A (0.4-0.7%). Many steviol glycosides are potent, non-nutritive sweeteners. Steviol glycosides comprise a diterpene core (formula I) substituted at R1 and R2 with various combinations of hydrogen, glucose, rhamnose, and xylose. Formula I [05] For example, R1 may be hydrogen, 1-ß-D-glucopyranosyl, or 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, and R2 may be hydrogen, 1-ß-D-glucopyranosyl, 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, or 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. Rebaudioside A (wherein R1 = 1-ß-D-glucopyranosyl and R2 = 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl) has a sweetness of about 200 to 300 times the sweetness of sucrose. The food industry has become interested in steviol glycosides in the pursuit of alternative sweeteners. However, the straight replacement of nutritive sweeteners with known potent non-nutritive sweeteners encounters problems of off-tastes, for example slow on-set, or bitter, licorice, or lingering aftertaste. These off-tastes also arise when steviol glycosides are used as non-nutritive sweeteners in food and beverage products. Thus, there is a need for additional alternative non-nutritive sweeteners. [06] It is therefore an object of at least certain embodiments of the present invention to provide compounds that are useful as sweeteners. It is an object of at least certain embodiments of the invention to provide beverage products or food products having alternative nutritional characteristics and taste properties. These and other objects, features and advantages of the invention or of certain embodiments of the invention will be apparent to those skilled in the art from the following disclosure and description of exemplary embodiments. BRIEF SUMMARY OF THE INVENTION [07] A family of new steviol glycoside isomers has now been discovered. In these isomers, the exo-cyclic double bond of formula I has been moved to an endo-cyclic position within the five-membered ring (see Formula II). These compounds are useful as sweeteners, and can be included as such in food and beverage products. In accordance with a first aspect of the invention, a compound is provided having formula II: Formula II [08] Wherein R1 may be hydrogen, 1-ß-D-glucopyranosyl, or 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, and R2 may be hydrogen, 1-ß-D-glucopyranosyl, 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, or 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. In certain exemplary embodiments, the compound of formula II may be isolated and purified. As used herein, “isolated and purified” means that the purity of the steviol glycoside isomer is at least 90 %. [09] In accordance with other aspects, a beverage product is provided comprising an aqueous liquid and a compound of formula II. [10] In accordance with other aspects, a food product is provided comprising a food component and a compound of formula II. [11] In accordance with another aspect of the invention, a sweetener is provided comprising a compound of formula II. [12] In accordance with another aspect, a method is provided for preparing the compounds of formula II, comprising the steps of providing an acidic aqueous solution comprising a compound of formula I, and heating the acidic aqueous solution to a temperature within the range of 30°C to 90°C for a period of time greater than two days. In certain exemplary embodiments, an acidic aqueous solution comprising rebaudioside A is heated to a temperature within the range of 40°C to 50°C at a pH within the range of pH 1.0 – 4.0 for a period of time greater than two days. BRIEF DESCRIPTION OF THE FIGURES [13] Figure 1 is a proton NMR spectrum of rebaudioside A. [14] Figure 2 is a proton NMR spectrum of iso-rebaudioside A. [15] Figure 3 is an overlay of the spectra from Figures 1 and 2. [16] Figure 4 is an ESI mass spectrum of rebaudioside A. [17] Figure 5 is an ESI mass spectrum of iso-rebaudioside A. [18] Figure 6 is an HPLC chromatogram of a 10-week reaction mixture containing rebaudioside A and iso-rebaudioside A. [19] Figure 7 is an ESI mass spectrum of the iso-rebaudioside A peak from Figure 6. [20] Figure 8 is an HPLC chromatogram of rebaudioside A. [21] Figure 9 is an HPLC chromatogram of iso-rebaudioside A. [22] Figure 10 is ESI mass spectrum of the rebaudioside A peak from Figure 8. [23] Figure 11 is ESI mass spectrum of the iso-rebaudioside A peak from Figure 9. [24] Figure 12 is an HPLC chromatogram of a 10-week reaction mixture enriched with isolated iso-rebaudioside A. [25] Figure 13 is ESI mass spectrum of the iso-rebaudioside A peak from Figure 12. [26] Figure 14 is an x-ray crystal structure of iso-rebaudioside A [27] Figure 15 is an x-ray crystal structure of rebaudioside A [28] Figure 16 is a comparison of the structures of rebaudioside A and iso-rebaudioside A [29] Figures 17 and 18 show the pH dependency of the rate of iso-rebaudioside A (Cmpd X) synthesis from rebaudioside A (Reb A). [30] Figure 19 shows the temperature dependency of the rate of iso-rebaudioside A (Cmpd X) synthesis from rebaudioside A (Reb A). [31] Figure 20 is a proton NMR spectrum of rebaudioside B. [32] Figure 21 is a proton NMR spectrum of iso-rebaudioside B. [33] Figure 22 is an overlay of the spectra from Figures 20 and 21. [34] Figure 23 is an overlay of HPLC chromatograms of rebaudioside B, iso-rebaudioside B, and a 1:1 mixture of the two compounds. DETAILED DESCRIPTION OF CERTAIN EXEMPLARY EMBODIMENTS [35] In certain exemplary embodiments, steviol glycoside isomers of the present invention may be defined by the general formula II: Formula II [36] Wherein R1 may be hydrogen, 1-ß-D-glucopyranosyl, or 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, and R2 may be hydrogen, 1-ß-D-glucopyranosyl, 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, or 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. Certain exemplary embodiments comprise compounds of formula II wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-rebaudioside A), R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-stevioside), R1 is hydrogen and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-rebaudioside B), R1 is hydrogen and R2 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-steviolbioside), R1 is 1-ß-D-glucopyranosyl and R2 is 1-ß-D-glucopyranosyl (iso-rubusoside), R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl (iso-dulcoside A), R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranose (iso-rebaudioside C), R1 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-rebaudioside D), R1 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl and R2 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-rebaudioside E), R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-rebaudioside F), R1 is hydrogen and R2 is 1-ß-D-glucopyranosyl (iso-steviolmonoside), or R1 is 1-ß-D-glucopyranosyl and R2 is hydrogen (iso-steviol II glucosyl ester). One exemplary embodiment comprises the compound of formula II wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. This compound has the structure shown in Formula III below. Hereinafter, this compound is referred to as iso-rebaudioside A. Formula III [37] In certain exemplary embodiments, steviol glycoside isomers disclosed here may be prepared by heating rebaudioside A in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce iso-rebaudioside A (Formula III). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the rebaudioside A starting material is converted to iso-rebaudioside A. A literature report suggests that under acidic conditions (pH 2.4 to 2.6) stevioside or rebaudioside A are quite stable at 60°C, but undergo drastic changes at 100°C, yielding hydrolysis byproducts such as glucose, steviolbioside (from stevioside), rebaudioside B (from rebaudioside A), and unknown compounds which have TLC Rf’s or HPLC tR’s very far removed from stevioside or rebaudioside A. When stevioside was subjected to high temperatures, isosteviol was also formed (Formula IV). (S.S. Chang and J. M. Cook, J. Agric. Food Chem., 31, 409 – 412 (1983)). Formula IV [38] Other literature reports have indicated that the acid-catalyzed hydrolysis of stevioside yields isosteviol (M. Bridel and R. Lavieille, Journal de Pharmacie et de Chimie, 14, 321 -328, and 369 -379 (1931), and J.R. Hanson and B.H. Oliverira, Natural Product Reports, 10, 301-309 (1993)). Isosteviol has been shown to be a Wagner-Meerwein rearrangement product involving inversion of the D-ring of steviol (Formula I wherein R1 and R2 each is hydrogen). Literature teachings thus suggest that steviol glycosides, e.g., rebaudioside A, would each undergo an acid-catalyzed isomerization, to a resultant product likewise having isosteviol as the aglycone moiety. [39] But surprisingly, it has now been found that acid and heat treatment of steviol glycosides, e.g., rebaudioside A, according to the present invention produces steviol glycoside isomers of Formula II, e.g., iso-rebaudioside A (Formula III), which have an aglycone moiety that is neither steviol nor isosteviol, but rather a new aglycone moiety having a migrated double bond in comparison to steviol. The unexpected aglycone moiety of the new compound is hereinafter called iso-steviol II (see Formula II). When R1 and R2 of Formula II are each hydrogen, the compound is called iso-steviol II (Formula V). Formula V [40] In certain exemplary embodiments, steviol glycoside isomers disclosed here may be hydrolyzed to remove glucose, rhamnose, and/or xylose units. Thus, steviol glycoside isomers, e.g., iso-rebaudiosides A-F, iso-stevioside, iso-dulcoside, etc., can be hydrolyzed upon further treatment with heat and acid into various other steviol glycoside isomers, e.g., iso-stevioside, iso-rebaudioside B, iso-steviolbioside, iso-rubusoside, iso-steviolmonoside, iso-steviol II glucosyl ester, etc. Thus, as a non-limiting example, rebaudioside A may be isomerized by treatment with heat and acid to iso-rebaudioside A as an intermediate, which may then be hydrolyzed to iso-rebaudioside B. In certain exemplary embodiments, steviol glycoside starting materials may be first hydrolyzed to remove one or more glucose, rhamnose, and/or xylose units, and then isomerized to steviol glycoside isomers. As a non-limiting example, rebaudioside A may be hydrolyzed by treatment with heat and acid to rebaudioside B as an intermediate, which may then be isomerized to iso-rebaudioside B. [41] In certain exemplary embodiments, an acidic aqueous solution having a pH within the range of pH 1.0 – 4.0 (e.g., within the range of pH 2.0 – 2.5) and comprising rebaudioside A (i.e., the compound of formula I wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl) is heated to a temperature within the range of 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce iso-rebaudioside B (i.e., the compound of formula II wherein R1 is hydrogen and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl). In one exemplary embodiment, under the above conditions rebaudioside A is first converted to iso-rebaudioside A, which is then converted to iso-rebaudioside B. In another exemplary embodiment, under the above conditions rebaudioside A is converted to rebaudioside B, which is then converted to iso-rebaudioside B. In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the rebaudioside A starting material is converted to iso-rebaudioside B. [42] In other exemplary embodiments, each of the steviol glycoside isomers disclosed herein may be prepared by treating a suitable steviol glycoside, e.g. the corresponding steviol glycoside, with acid and heat according to the method of invention. Specifically, stevioside may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-stevioside). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the stevioside starting material is converted to iso-stevioside. Similarly, rebaudioside B may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is hydrogen and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-rebaudioside B). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the rebaudioside B starting material is converted to iso-rebaudioside B. Steviolbioside may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is hydrogen and R2 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-steviolbioside). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the steviolbioside starting material is converted to iso-steviolbioside. Rubusoside may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is 1-ß-D-glucopyranosyl and R2 is 1-ß-D-glucopyranosyl (iso-rubusoside). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the rubusoside starting material is converted to iso-rubusoside. Steviolmonoside may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is hydrogen and R2 is 1-ß-D-glucopyranose (iso-steviolmonoside). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the steviolmonoside starting material is converted to iso-steviolmonoside. Steviol glucose ester (Formula I wherein R1 is 1-ß-D-glucopyranosyl and R2 is hydrogen) may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is 1-ß-D-glucopyranose and R2 is hydrogen (iso-steviol II glucosyl ester). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the steviol glucose ester starting material is converted to iso-steviol II glucosyl ester. Dulcoside A may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl (iso-dulcoside A). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the dulcoside A starting material is converted to iso-dulcoside A. Rebaudioside C may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranose (iso-rebaudioside C). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the rebaudioside C starting material is converted to iso-rebaudioside C. Rebaudioside D may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-rebaudioside D). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the rebaudioside D starting material is converted to iso-rebaudioside D. Rebaudioside E may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl and R2 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-rebaudioside E). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the rebaudioside E starting material is converted to iso-rebaudioside E. Rebaudioside F may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., 43°C, 65°C, 75°C, 85°C, or within the range of about 40°C to about 50°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a compound of formula II wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl (iso-rebaudioside F). In certain exemplary embodiments, at least 1.0 % by weight (e.g., at least 5%, at least 10%, at least 25%, at least 40%, at least 50%, at least 75%, at least 90% by weight) of the rebaudioside F starting material is converted to iso-rebaudioside F. Other synthesis methods may be employed, for example enzymatic isomerization. Steviol glycoside isomers may be isolated and purified, e.g., by chromatography, recrystallization, etc. [43] Exemplary acids suitable for use in preparing steviol glycoside isomers under strongly acidic conditions include inorganic acids such as phosphoric acid, hydrochloric acid, nitric acid, sulfuric acid, etc. and/or organic acids such as citric acid, malic acid, tartaric acid, lactic acid, ascorbic acid, etc. One or more acids, and optionally the corresponding acid salt (e.g. citric acid and citrate), are included in the reaction mixture in an amount sufficient to render the reaction mixture strongly acidic (e.g., to achieve a pH value within the range of about pH 1.0 – 4.0, such as about pH 2.0 - 2.5). Enzymatic isomerization may also be employed. [44] Steviol glycosides of Formula I, singularly or as a mixture, can have an additional number of ß-D-glucopyranosyl units covalently bonded 4?1 to existing ß-D-glucopyranosyl units at R1 and/or R2 via enzymatic transglucosylation reactions with starch, yielding a complex mixture of products. (See Kazuhiro Ohtani and Kazuo Yamasaki, Chapter 7, “Method to improve the taste of the sweet principles of Stevia rebaudiana,” p. 145 in the book entitled “Stevia, The genus Stevia”, edited by A. Douglas Kinghorn, Taylor & Francis, 2002). These enzyme-modified Stevia extracts are commercially available for use as sweeteners in food and beverage products. Steviol glycoside isomers of Formula II may be subjected to the same kind of enzymatic transglucosylation reactions, yielding a complex mixture of products that are useful as sweeteners for food and beverage products. It is also contemplated that the product of enzymatic transglucosylation of the steviol glycosides of Formula I may be heated in aqueous solution to a temperature within the range of about 30°C to about 90°C (e.g., within the range of about 40°C to about 50°C, such as 43°C) under strongly acidic conditions (e.g. about pH 1.0 – 4.0; such as about pH 2.0 – 2.5) for a sufficient period of time (e.g., greater than two days, such as from two days to about 11 weeks) to produce a complex mixture of products having the aglycone moiety of Formula II. These isomerization products may also be useful as sweeteners in food and beverage products. [45] In certain exemplary embodiments, steviol glycoside isomers comprising at least one compound of Formula II may be used as a potent non-nutritive sweetener. Sweeteners are edible consumables suitable for consumption and for use in foods and beverages. As used herein, "edible consumables" means a food or beverage or an ingredient of a food or beverage for human or animal consumption. As used herein, a “non-nutritive sweetener” is one which does not provide significant caloric content in typical usage amounts, e.g., one which imparts less than 5 calories per 8 oz. serving of beverage to achieve the sweetness equivalent of 10 Brix of sugar. As used herein, a “potent sweetener” means a sweetener which is at least twice as sweet as sugar (sucrose), that is, a sweetener which on a weight basis requires no more than half the weight of sugar to achieve an equivalent sweetness. For example, a potent sweetener may require less than one-half the weight of sugar to achieve an equivalent sweetness in a beverage sweetened to a level of 10 degrees Brix with sugar. [46] In certain exemplary embodiments, a sweetener may comprise at least one compound of formula II, and optionally a filler, a bulking agent such as dextrose, maltodextrin, erythritol, tagatose, or erythritol and tagatose blend, polydextrose, and/or an anti-caking agent. [47] In certain exemplary embodiments, one or more of the steviol glycoside isomers disclosed here may be present as a non-nutritive sweetener in a beverage product. In certain exemplary embodiments, the beverage product includes a sweetening amount of iso-rebaudioside A (i.e., the compound of formula II wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl). In certain exemplary embodiments, the beverage product includes at least 0.005 % by weight (e.g., at least 0.01%, at least 0.02%, at least 0.03% by weight) of iso-rebaudioside A. In certain exemplary embodiments, the beverage product includes a sweetening amount of iso-rebaudioside B (i.e., the compound of formula II wherein R1 is hydrogen and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl). In certain exemplary embodiments, the beverage product includes at least 0.005 % by weight (e.g., at least 0.01%, at least 0.02%, at least 0.03% by weight) of iso-rebaudioside B. [48] Exemplary beverage products comprise an aqueous liquid and a compound of formula II, and include beverages such as, for example, ready to drink liquid formulations, beverage concentrates and the like. Beverages include, e.g., carbonated and non-carbonated soft drinks, fountain beverages, frozen ready-to-drink beverages, frozen carbonated beverages, liquid concentrates, powdered concentrates, coffee beverages, tea beverages, dairy beverages, flavored waters, enhanced waters, fruit juice, fruit juice-flavored drinks, fruit-flavored drinks, sports drinks, soy drinks, vegetable drinks, grain-based drinks (e.g. malt beverages), fermented drinks (e.g., yogurt and kefir), alcoholic beverages, and mixtures of any of them. Exemplary fruit juice sources include citrus fruit, e.g. orange, grapefruit, lemon and lime, berry, e.g. cranberry, raspberry, blueberry and strawberry, apple, grape, pineapple, prune, pear, peach, cherry, mango, and pomegranate. Beverage products include bottle, can, and carton products and fountain syrup applications. [49] The terms "beverage concentrate" and "syrup" are used interchangeably throughout this disclosure. At least certain exemplary embodiments of the beverage concentrates contemplated are prepared with an initial volume of water to which the additional ingredients are added. Full strength beverage compositions can be formed from the beverage concentrate by adding further volumes of water to the concentrate. Typically, for example, full strength beverages can be prepared from the concentrates by combining approximately 1 part concentrate with between approximately 3 to approximately 7 parts water. In certain exemplary embodiments the full strength beverage is prepared by combining 1 part concentrate with 5 parts water. In certain exemplary embodiments the additional water used to form the full strength beverages is carbonated water. In certain other embodiments, a full strength beverage is directly prepared without the formation of a concentrate and subsequent dilution. [50] In certain exemplary embodiments, one or more of the steviol glycoside isomers disclosed here may be present as a non-nutritive sweetener in a food product. Food products comprise at least one food component, i.e., any edible material suitable for human or animal consumption, whether or not fully or partially digestible. Non-limiting examples of food components include proteins, carbohydrates, fats, vitamins, minerals, etc. Food products comprising a compound of formula II disclosed here include, e.g., oatmeal, cereal, baked goods (e.g., cookies, crackers, cakes, brownies, breads, etc.), snack foods (e.g., potato chips, tortilla chips, popcorn, snack bars, rice cakes, etc.), and other grain-based food products. All variations, alternatives, options, etc., discussed elsewhere in this disclosure apply to food embodiments of the invention. [51] It should be understood that food or beverage products in accordance with this disclosure may have any of numerous different specific formulations or constitutions. The formulation of a food or beverage product in accordance with this disclosure can vary to a certain extent, depending upon such factors as the product’s intended market segment, its desired nutritional characteristics, flavor profile and the like. For example, it will generally be an option to add further ingredients to the formulation of a particular food or beverage embodiment, including any of the food or beverage formulations described herein. Additional (i.e., more and/or other) sweeteners may be added. Acidulants, flavorings, colorings, electrolytes, minerals, non-mineral nutritional supplements, fruit juices or other fruit products, tastents, masking agents and the like, flavor enhancers, buffering agents, thickeners, emulsifiers, edible particulates, anti-foaming agents, preservatives, carbonation, and mixtures thereof typically can be added to any such formulations to vary the taste, mouthfeel, nutritional characteristics, functionality, etc. of the food or beverage product. Examples of non-mineral nutritional supplement ingredients are known to those of ordinary skill in the art and include, for example, antioxidants and vitamins, including Vitamins A, D, E (tocopherol), C (ascorbic acid), B (thiamine), B2 (riboflavin), B6, B12, and K, niacin, folic acid, biotin, and combinations thereof. The optional non-mineral nutritional supplements are typically present in amounts generally accepted under good manufacturing practices. Exemplary amounts are between about 1% and about 100% RDV (recommended daily value), where such RDV are established. In certain exemplary embodiments the non-mineral nutritional supplement ingredient(s) are present in an amount of from about 5% to about 20% RDV, where established. Additional and alternative suitable ingredients will be recognized by those skilled in the art given the benefit of this disclosure. [52] Certain exemplary embodiments of carbonated beverages disclosed here are cola flavored carbonated beverages, which characteristically comprise carbonated water, a compound of formula II, kola nut extract and/or other cola flavoring, caramel coloring, an acidulant (e.g. phosphoric acid), and optionally other ingredients such as other sweeteners. Certain other exemplary embodiments of carbonated beverages disclosed here are citrus flavored (e.g., lemon-lime, grapefruit, lemon, lime, etc.) carbonated beverages, which characteristically comprise carbonated water, a compound of formula II, citrus flavoring, an acidulant (e.g. citric acid), and optionally other ingredients such as coloring agents and/or other sweeteners. In certain exemplary embodiments, a beverage concentrate is provided comprising water, a compound of formula II, cola flavoring, caramel coloring, and acidulant (e.g., phosphoric acid), and optionally other ingredients such as other sweeteners. In certain exemplary embodiments, a beverage concentrate is provided comprising water, a compound of formula II, citrus flavoring, an acidulant (e.g., citric acid), and optionally other ingredients such as coloring agents and /or other sweeteners. [53] In at least certain exemplary embodiments of the food and beverage products disclosed herein, additional/other sweeteners may be included, for example, nutritive sweeteners or non-nutritive sweeteners. Non-limiting examples of nutritive sweeteners include sucrose, liquid sucrose, fructose, liquid fructose, glucose, liquid glucose, glucose-fructose syrup from natural sources such as apple, chicory, agave, honey, etc., e.g., high fructose corn syrup, chicory syrup, Agave syrup, invert sugar, medium invert sugar, maple syrup, maple sugar, honey, brown sugar molasses, e.g., cane molasses and sugar beet molasses, sorghum syrup, an mixtures of any of them. Such sweeteners are present in at least certain exemplary embodiments in an amount of from about 0.1% to about 20% by weight of the finished food or beverage product, such as from about 6% to about 16% by weight, depending upon the desired level of sweetness for the finished food or beverage product. Nutritive sweeteners may be present in beverage concentrate embodiments up to about 60% by weight of the beverage concentrate. [54] Non-limiting examples of potent non-nutritive natural sweeteners that may be included in food and beverage products include rebaudioside A, stevioside, other steviol glycosides, Stevia rebaudiana extracts, Lo Han Guo (LHG), e.g., LHG juice concentrate or LHG powder, thaumatin, monellin, brazzein, monatin, and mixtures of any of them. LHG, if used, may have for example, mogroside V content of from about 2 to about 99%. In certain exemplary embodiments, a food or beverage product is provided which comprises a mixture of a compound of formula II and LHG having a mogroside V content of at least 30%. In certain exemplary embodiments, the LHG in the mixture has a mogroside V content of about 45%, plus or minus 5%. In certain exemplary embodiment, a mixture comprising LHG and a compound of formula II provides at least 10% of the sweetness in a food or beverage product. In certain exemplary embodiments, the mixture provides about 1/3 to about 2/3 of the sweetness. Other examples of non-nutritive sweeteners include sorbitol, mannitol, xylitol, glycyrrhizin, maltitol, maltose, lactose, xylose, arabinose, isomalt, lactitol, trehalulose, ribose, fructo-oligosaccharides, and mixtures of any of them. Optionally, the sweetener component can include erythritol, tagatose, an erythritol and tagatose blend, or polydextrose. In certain exemplary embodiments, a food or beverage product is provided which comprises a compound of formula II and either erythritol, tagatose, or a blend of erythritol and tagatose. [55] Non-limiting examples of potent non-nutritive artificial sweeteners that may be included in food and beverage products include peptide based sweeteners, e.g., aspartame, neotame, and alitame, and non-peptide based sweeteners, e.g., sodium saccharin, calcium saccharin, acesulfame (including but not limited to acesulfame potassium), cyclamate (including but not limited to sodium cyclamate and/or calcium cyclamate), neohesperidin dihydrochalcone, sucralose, and mixtures of any of them. Potent non-nutritive sweeteners typically are employed at a level of milligrams per ounce of food or beverage according to their sweetening power, any applicable regulatory provisions of the country where the food or beverage is to be marketed, the desired level of sweetness of the food or beverage, etc. Mixtures of any of the above nutritive and non-nutritive sweeteners are included within the scope of the disclosed invention. It will be within the ability of those skilled in the art, given the benefit of this disclosure, to select suitable additional or alternative sweeteners for use in various embodiments of the food and beverage products disclosed here. [56] Those of ordinary skill in the art will understand that, for convenience, some ingredients are described here in certain cases by reference to the original form of the ingredient in which it is added to the beverage product formulation. Such original form may differ from the form in which the ingredient is found in the finished food or beverage product. Thus, for example, in certain exemplary embodiments of the cola beverage products of this disclosure, sucrose and liquid sucrose would typically be substantially homogenously dissolved and dispersed in the beverage. Likewise, other ingredients identified as a solid, concentrate (e.g., juice concentrate), etc. would typically be homogenously dispersed throughout the food or beverage product, rather than remaining in their original form. Thus, reference to the form of an ingredient of a food or beverage product formulation should not be taken as a limitation on the form of the ingredient in the food or beverage product, but rather as a convenient means of describing the ingredient as an isolated component of the product formulation. [57] In at least certain exemplary embodiments, food and beverage products disclosed here may be preserved by pasteurization. The pasteurization process may include, for example, ultra high temperature (UHT) treatment and/or high temperature-short time (HTST) treatment. The UHT treatment includes subjecting the food or beverage product to high temperatures, such as by direct steam injection or steam infusion, or by indirect heating in a heat exchanger. Generally, after the product is pasteurized, the product can be cooled as required by the particular product composition/configuration and/or the package filling application. For example, in one embodiment, the food or beverage product is subjected to heating to about 85°C to about 121°C for a short period of time, for example, about 1 to 60 seconds, then cooled quickly to about 2.2°C +/- 2.8°C) for refrigerated products, to ambient temperature for shelf stable or refrigerated products, and to about 85°C +/- 5.5°C for hot-fill applications for shelf-stable products. The pasteurization process is typically conducted in a closed system, so as not to expose the food or beverage product to atmosphere or other possible sources of contamination. Other pasteurization or sterilization techniques may also be useful, such as, for example, aseptic packaging, tunnel pasteurization, or retort processing. In general, tunnel pasteurization methods typically use lower temperatures for a longer time, e.g., about 71°C for 10-15 minutes, and retort methods typically use, e.g., about 121°C for 3-5 minutes at elevated pressure, i.e., at pressure above 1 atmosphere. In addition, multiple pasteurization processes may be carried out in series or parallel, as necessitated by the food or beverage product or ingredients. [58] The following examples are specific embodiments of the present invention but are not intended to limit it. EXAMPLE 1 [59] Synthesis of iso-rebaudioside A: Rebaudioside A (0.5 g) dissolved in an aqueous citrate buffer solution (about pH 2.0) was heated for 10 weeks at about 43.3°C. The reaction mixture was then freeze-dried and then subjected to a silica gel column (1 x 20 cm) eluting with a solvent system of 70% acetone, 15% triethylamine, and 15% water. Two fractions were isolated, with fraction 2 containing rebaudioside A and iso-rebaudioside A. After concentration, approximately 6 mg of oil was isolated from fraction 2. The oil was dissolved in D2O (0.6 mL) and left at room temperature for about three days. Clear, colorless needle crystals (1-2 mg) formed and were isolated for analysis. EXAMPLE 2 [60] Analysis of iso-rebaudioside A: [61] A small amount of the crystalline product of Example 1 was analyzed by proton NMR and compared to the parent rebaudioside A spectrum (D2O, 400 MHz 1H-NMR). The two compounds were not identical, which showed that a new isomer had formed. Figures 1 and 2 contain the proton NMR spectra of a rebaudioside A standard and iso-rebaudioside A, respectively. Figure 3 shows an overlay of the two spectra. [62] Samples of rebaudioside A standard and the crystalline product of Example 1 were submitted for mass spectral analysis (ESI positive ion mode). Both compounds showed the expected molecular weight for rebaudioside A of 966.5 amu and similar fragmentation patterns. Figures 4 and 5 show the mass spectra of rebaudioside A and iso-rebaudioside A, respectively. [63] Analyses were performed on a C-18 reverse-phase analytical column (Alltima 2.1 x 250 mm) at a flow rate of 0.250 mL/min with detection at 210 nm, and evaporative light scattering (ELSD) detection. The column was pre-quilibrated with water containing 0.1% trifluoroacetic acid (solvent A). Solvent B was acetonitrile containing 0.1% trifluoroacetic acid. The gradient conditions were: Time (min) Solvent A% Solvent B% 0 100 0 3 100 0 35 5 95 40 5 95 41 0 00 50 0 100 [64] The product of Example 1 was injected in water (5 µL), resulting in two peaks in a 30:70 ratio that were not baseline resolved, the minor peak eluting at 22.523 minutes and the major peak eluting at 22.680 minutes. A rebaudioside A standard was run on the HPLC under the same conditions and proved to be the peak eluting at 22.523 min. The same rebaudioside A standard was enriched with a small amount of the crystalline product of Example 1, and when run on the HPLC revealed a proportionally increased peak area at 22.680 minutes. [65] Rebaudioside A and its isomer were baseline resolved by injecting the crude 10 week reaction mixture of Example 1 onto the same C-18 reverse-phase column, eluting with an isocratic mixture consisting of 30:70 acetonitrile:water with 0.1% formic acid, at a flow rate of 0.25 mL/min. Baseline resolution was also obtained using a 15 minute gradient of 95% water to acetonitrile at a flow rate of 0.25 mL/min. Under these conditions, rebaudioside A eluted at about 10.9 minutes, and iso-rebaudioside A eluted at about 12.2 minutes (Figure 6). Detection by LC/MS (ESI-MS) exhibited a molecular ion of 989 (M+23, the Na ion adduct) for the iso-rebaudioside A peak at 12.2 minutes (Figure 7). A rebaudioside A standard and isolated iso-rebaudioside A were analyzed separately by LC/MS. The rebaudioside A standard eluted at 11.08 minutes (Figure 8), corresponding to the 10.9 minute peak in Figure 6, and the isolated iso-rebaudioside A eluted at 12.1 minutes (Figure 9), corresponding to the 12.2 minute peak in Figure 6. Both the standard and the isolated product had a molecular ion of 989 (Figures 10 and 11, respectively). A mixture of crude 10 week reaction mixture from Example 1 enriched with isolated iso-rebaudioside A was analyzed by LC/MS. The added iso-rebaudioside A co-eluted with and increased the area of the peak at 12.2 minutes (Figure 12, compare with Figure 6), and mass spectrum of the 12.2 minute peak still gave a molecular ion of 989 (Figure 13). [66] The NMR, HPLC, and mass spectral data together unambiguously confirmed that the new compound iso-rebaudioside A was a chemically distinct derivative of rebaudioside A. EXAMPLE 3 [67] Synthesis of iso-rebaudioside A: Rebaudioside A (5 g) was dissolved in an aqueous solution of citrate buffer (pH 2, 100 mM, 200 mL) and heated to about 75°C. The reaction progress was monitored via HPLC and when the ratio of iso-rebaudioside A to rebaudioside A was greater than 75% (72 hours) the reaction mixture was evaporated to a sticky crystalline solid. The product mixture was passed through a silica column (10 x 40 cm) eluting with acetone:water:triethylamine (70:15:15) to provide a glassy oil (about 1.0 g). Analysis by HPLC showed the presence of rebaudioside A and iso-rebaudioside A along with a large amount of apparently hydrolyzed material corresponding to the loss of one or more sugar moieties (e.g., iso-stevioside, iso-rebaudioside B, iso-rubusoside, iso-steviolbioside, iso-steviolmonoside, etc.). [68] The glassy oil was dissolved in water (3 mL) and separated by semi-preparative HPLC (Alltech Alltima C-18 semi-preparative column, 10 x 250 mm, flow rate 5 mL/min, solvent composition 30% acetonitrile in water with 0.1% formic acid). Repeated injections, 15 in all, were made and a peak eluting at 13.7 minutes was collected, the fractions pooled and concentrated to a white powder (23 mg of isolated and purified iso-rebaudioside A). The white powder was first suspended in water (2 mL) and centrifuged. The residual solid was dissolved in warm acetonitrile (200 µL) followed by the addition of water (200 µL) and allowed to sit at room temperature for 5 days whereupon crystals in the form of large needles slowly appeared. The mixture was submitted for x-ray crystallography without perturbing the crystals. The crystals were separated from the liquid portion, and the two samples were dried separately under high vacuum for three days. The dried crystals were used to obtain X-ray crystallography data. [69] An x-ray crystal structure of iso-rebaudioside A was obtained and the structure was elucidated (see Figure 14). For comparison, an x-ray crystal structure was obtained for rebaudioside A standard, and the structure was elucidated (Figure 15). X-ray crystallography analysis unexpectedly showed that the three-dimensional structure of iso-rebaudioside A has an endocyclic double bond in the five-membered ring, with an external methyl group, as evidenced by the shorter bond length between carbons 15 and 16. The crystal structure of rebaudioside A showed the expected exocyclic double bond, as evidenced by the shorter bond length between carbons 15 and 17. See Figure 16 for a comparison of bond lengths. So surprisingly, the structure of iso-rebaudioside A was shown to be a product of acid-catalyzed double bond migration, and not a product of Wagner-Meerwein rearrangement as predicted based on literature reports wherein under heat and acidic conditions steviol was converted to isosteviol. EXAMPLE 4 [70] Iso-rebaudioside A from the x-ray crystallography sample of Example 3 was dissolved in water at a concentration of 1000 ppm, and was found by a panel of five people to have a sweetness intensity similar to that of a 7% sucrose solution; therefore its sweetness potency was estimated to be 70 times that of sucrose. EXAMPLE 5 [71] Six reactions were set up under identical conditions as in Example 3 except for temperatures: 43°C, 65°C, 75°C, 85°C, and 90°C reactions were set up and followed by HPLC-MS or UV (210 nm) detection. It was observed that at elevated temperatures extensive hydrolysis occurred with the largest part of rebaudioside A being hydrolyzed, removing one or more sugar moieties as determined by HPLC-MS analysis as the reaction proceeded. EXAMPLE 6 [72] Two studies were performed on the pH dependency of the synthesis of iso-rebaudioside A (Cmpd X) from rebaudioside A (Reb A). Rebaudioside A was dissolved at the same concentration in a series of aqueous citric acid solutions, each having a different pH. The solutions were heated to 43°C for 11 weeks. One study was performed with solutions at pH 2.0, 4.0, and 7.0. The other study was performed with solutions at pH 2.5, 3.0, and 3.5. Results of the two studies are shown in Figures 17 and 18, respectively, wherein Reb A stands for rebaudioside A and Cmpd X stands for iso-rebaudioside A. In Figure 17, the concentration of iso-rebaudioside A at pH 2 peaks at week 9 and decreases afterwards. The concentration of rebaudioside A at pH 2 continues to decrease after week 9. This indicates that iso-rebaudioside A itself is being degraded/hydrolyzed into other steviol glycoside isomers, e.g. iso-rebaudioside B, etc. EXAMPLE 7 [73] A study was performed on the temperature dependency of the synthesis of iso-rebaudioside A (Cmpd X) from rebaudioside A (Reb A). Rebaudioside A was dissolved at the same concentration in a series of aqueous citric acid solutions, all at pH 2.5. Each of the solutions was kept at a different temperature (21°C, 32°C, and 43°C) for 11 weeks. Results of the study are shown in Figure 19. EXAMPLE 8 [74] Iso-rebaudioside B (Formula VI) was synthesized and purified according to the procedure set forth in Example 3, under reaction conditions more favorable to the formation of iso-rebaudioside B. Such reaction conditions include a longer reaction time and/or a higher reaction temperature than those of Example 3. The iso-rebaudioside B was purified by semi-preparative HPLC, and the purified iso-rebaudioside B was analyzed by proton NMR and compared with the NMR spectrum of a rebaudioside B reference sample (D2O, 400 MHz 1H-NMR). Figures 20 and 21 show the proton NMR spectra of a rebaudioside B standard and iso-rebaudioside B, respectively, with expanded sections to show detail. Figure 22 shows an overlay of the two NMR spectra. Figure 22 shows two readily discernable differences between the two compounds. The iso-rebaudioside B spectrum has three methyl group singlets while the rebaudioside B spectrum has only two. Also, in the alkenyl region around 5.2 ppm, the two-proton alkenyl peak for rebaudioside B is slightly downfield of the one-proton peak of iso-rebaudioside B. [75] Analyses were performed on reverse-phase analytical HPLC according to the procedure set forth in Example 2. Figure 23 shows an overlay of HPLC traces for three samples: a rebaudioside B standard, iso-rebaudioside B, and a 1:1 mixture of the two. Figure 23 shows that the peaks for rebaudioside B and iso-rebaudioside B are not baseline separated under these conditions, but can be distinguished. UV-VIS and mass spectra are essentially identical for the two compounds. The iso-rebaudioside B isolated from the reaction mixture appears to still have approximately 26% rebaudioside B after comparing HPLC traces and NMR spectra for the two compounds. [76] The invention has been described with reference to the preferred embodiments. Obviously, modifications and alterations will occur to those skilled in the art upon reading and understanding the preceding detailed description. It is intended that the invention be construed as including all such modifications and alterations insofar as they come within the scope of the appended claims or the equivalents thereof. WE CLAIM:- 1. A compound of formula II: (II) wherein R1 is hydrogen, 1-ß-D-glucopyranosyl, or 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, and R2 is hydrogen, 1-ß-D-glucopyranosyl, 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, or 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 2. The compound of claim 1, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 3. The compound of claim 1, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 4. The compound of claim 1, wherein R1 is hydrogen and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 5. The compound of claim 1, wherein R1 is hydrogen and R2 is 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 6. The compound of claim 1, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 1-ß-D-glucopyranosyl. 7. The compound of claim 1, wherein R1 is hydrogen and R2 is 1-ß-D-glucopyranosyl. 8. The compound of claim 1, wherein R1 is 1-ß-D-glucopyranosyl and R2 is hydrogen. 9. The compound of claim 1, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl. 10. The compound of claim 1, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 11. The compound of claim 1, wherein the compound is isolated and purified. 12. A beverage product comprising: an aqueous liquid, and a compound of formula II: (II) wherein R1 is hydrogen, 1-ß-D-glucopyranosyl, or 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, and R2 is hydrogen, 1-ß-D-glucopyranosyl, 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, or 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 13. The beverage product of claim 12, wherein the beverage product is selected from the group consisting of carbonated beverages, non-carbonated beverages, fountain beverages, frozen carbonated beverages, powdered concentrates, beverage concentrates, fruit juices, fruit juice-flavored drinks, fruit-flavored drinks, sports drinks, energy drinks, fortified/enhanced water drinks, soy drinks, vegetable drinks, grain-based drinks, malt beverages, fermented drinks, yogurt drinks, kefir, coffee beverages, tea beverages, dairy beverages, and mixtures of any of them. 14. The beverage product of claim 12, further comprising a sweetener selected from the group consisting of a steviol glycoside, Stevia rebaudiana extracts, Lo Han Guo, Lo Han Guo juice concentrate, Lo Han Guo powder, mogroside V, thaumatin, monellin, brazzein, monatin, erythritol, tagatose, sucrose, liquid sucrose, fructose, liquid fructose, glucose, liquid glucose, high fructose corn syrup, invert sugar, medium invert sugar, maple syrup, maple sugar, honey, chicory syrup, Agave syrup, brown sugar molasses, cane molasses, sugar beet molasses, sorghum syrup, sorbitol, mannitol, maltitol, xylitol, glycyrrhizin, malitol, maltose, lactose, xylose, arabinose, isomalt, lactitol, trehalulose, ribose, fructo-oligosaccharides, aspartame, neotame, alitame, sodium saccharin, calcium saccharin, acesulfame potassium, sodium cyclamate, calcium cyclamate, neohesperidin dihydrochalcone, sucralose, polydextrose, and mixtures of any of them. 15. The beverage product of claim 12, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, wherein the beverage product is a beverage concentrate, and further comprising rebaudioside A. 16. The beverage product of claim 12, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, wherein the beverage product is a carbonated beverage, and further comprising rebaudioside A. 17. The beverage product of claim 12, comprising a sweetening amount of the compound of formula II, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 18. The beverage product of claim 12, comprising at least 0.005 % by weight of the compound of formula II, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 19. The beverage product of claim 12, comprising a sweetening amount of the compound of formula II, wherein R1 is hydrogen and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 20. The beverage product of claim 12, comprising at least 0.005 % by weight of the compound of formula II, wherein R1 is hydrogen and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 21. A food product comprising: a food component, and a compound of formula II: (II) wherein R1 is hydrogen, 1-ß-D-glucopyranosyl, or 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, and R2 is hydrogen, 1-ß-D-glucopyranosyl, 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, or 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 22. The food product of claim 21, wherein the food product is selected from the group consisting of oatmeal, cereal, baked goods, cookies, crackers, cakes, brownies, breads, snack foods, potato chips, tortilla chips, popcorn, snack bars, rice cakes, and grain-based food products. 23. The food product of claim 21, further comprising a sweetener selected from the group consisting of a steviol glycoside, Stevia rebaudiana extracts, Lo Han Guo, Lo Han Guo juice concentrate, Lo Han Guo powder, mogroside V, thaumatin, monellin, brazzein, monatin, erythritol, tagatose, sucrose, liquid sucrose, fructose, liquid fructose, glucose, liquid glucose, high fructose corn syrup, invert sugar, medium invert sugar, maple syrup, maple sugar, honey, chicory syrup, Agave syrup, brown sugar molasses, cane molasses, sugar beet molasses, sorghum syrup, sorbitol, mannitol, maltitol, xylitol, glycyrrhizin, malitol, maltose, lactose, xylose, arabinose, isomalt, lactitol, trehalulose, ribose, fructo-oligosaccharides, aspartame, neotame, alitame, sodium saccharin, calcium saccharin, acesulfame potassium, sodium cyclamate, calcium cyclamate, neohesperidin dihydrochalcone, sucralose, polydextrose, and mixtures of any of them. 24. The food product of claim 23, wherein the steviol glycoside is rebaudioside A, and wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 25. A sweetener comprising a compound of formula II: (II) wherein R1 is hydrogen, 1-ß-D-glucopyranosyl, or 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, and R2 is hydrogen, 1-ß-D-glucopyranosyl, 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, or 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl. 26. The sweetener of claim 25, further comprising at least one of a filler, bulking agent, and an anticaking agent. 27. A method for preparing a compound of formula II: (II) wherein R1 is hydrogen, 1-ß-D-glucopyranosyl, or 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, and R2 is hydrogen, 1-ß-D-glucopyranosyl, 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, or 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, comprising the steps of: providing an acidic aqueous solution comprising a compound of formula I: (I) wherein R1 is hydrogen, 1-ß-D-glucopyranosyl, or 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, and R2 is hydrogen, 1-ß-D-glucopyranosyl, 2-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-1-ß-D-glucopyranosyl, 2-(1-a-L-rhamnopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl, or 2-(1-ß-D-xylopyranosyl)-3-(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl; and heating the solution to a temperature within the range of 30°C to 90°C for a period of time greater than two days. 28. The method of claim 27, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl in the compound of formula I. 29. The method of claim 28, wherein R1 is 1-ß-D-glucopyranosyl and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl in the compound of formula II; and the acidic aqueous solution has a pH value within the range of pH 1.0 – 4.0. 30. The method of claim 29, wherein at least 1.0 % by weight of the compound of formula I is converted to the compound of formula II. 31. The method of claim 28, wherein R1 is hydrogen and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl in the compound of formula II; and the acidic aqueous solution has a pH value within the range of pH 1.0 – 4.0. 32. The method of claim 31, wherein at least 1.0 % by weight of the compound of formula I is converted to the compound of formula II. 33. The method of claim 27, wherein R1 is hydrogen and R2 is 2,3-bis(1-ß-D-glucopyranosyl)-1-ß-D-glucopyranosyl in both the compound of formula I and the compound of formula II; and the acidic aqueous solution has a pH value within the range of pH 1.0 – 4.0. 34. The method of claim 33, wherein at least 1.0 % by weight of the compound of formula I is converted to the compound of formula II. 35. The method of claim 27, wherein the temperature is within the range of 40°C to 50°C, and the acidic aqueous solution further comprises at least one of phosphoric acid, hydrochloric acid, nitric acid, sulfuric acid, citric acid, malic acid, tartaric acid, lactic acid, and ascorbic acid, in an amount sufficient to achieve a pH value within the range of pH 1.0 – 4.0.

Documents:

413-MUMNP-2010-ABSTRACT(13-04-2010).pdf

413-MUMNP-2010-CHINESE DOCUMENT(13-3-2012).pdf

413-MUMNP-2010-CLAIMS(AMENDED)-(13-04-2010).pdf

413-MUMNP-2010-CLAIMS(AMENDED)-(6-3-2013).pdf

413-MUMNP-2010-CLAIMS(MARKED COPY)-(10-3-2014).pdf

413-MUMNP-2010-CLAIMS(MARKED COPY)-(6-3-2013).pdf

413-MUMNP-2010-CN DOCUMENT(10-9-2012).pdf

413-MUMNP-2010-CORRESPONDENCE(12-5-2010).pdf

413-MUMNP-2010-CORRESPONDENCE(13-04-2010).pdf

413-MUMNP-2010-CORRESPONDENCE(13-3-2012).pdf

413-MUMNP-2010-CORRESPONDENCE(21-5-2013).pdf

413-MUMNP-2010-CORRESPONDENCE(25-9-2012).pdf

413-MUMNP-2010-CORRESPONDENCE(27-7-2012).pdf

413-MUMNP-2010-CORRESPONDENCE(28-1-2013).pdf

413-MUMNP-2010-CORRESPONDENCE(3-3-2014).pdf

413-MUMNP-2010-CORRESPONDENCE(5-3-2010).pdf

413-MUMNP-2010-CORRESPONDENCE(8-9-2010).pdf

413-MUMNP-2010-ENGLISH TRANSLATION VERIFICATION(21-5-2013).pdf

413-MUMNP-2010-ENGLISH TRANSLATION(28-1-2013).pdf

413-MUMNP-2010-EP DOCUMENT(10-9-2012).pdf

413-MUMNP-2010-EP PATENT(6-3-2013).pdf

413-MUMNP-2010-FORM 1(25-9-2012).pdf

413-mumnp-2010-form 13(13-04-2010).pdf

413-MUMNP-2010-FORM 13(27-7-2012).pdf

413-MUMNP-2010-FORM 18(5-3-2010).pdf

413-MUMNP-2010-FORM 3(10-9-2012).pdf

413-MUMNP-2010-FORM 3(28-1-2013).pdf

413-MUMNP-2010-FORM 3(6-3-2013).pdf

413-MUMNP-2010-FORM 3(8-9-2010).pdf

413-MUMNP-2010-KOREAN DOCUMENT(10-9-2012).pdf

413-MUMNP-2010-MARKED COPY(13-04-2010).pdf

413-MUMNP-2010-OTHER DOCUMENT(10-3-2014).pdf

413-MUMNP-2010-OTHER DOCUMENT(3-3-2014).pdf

413-MUMNP-2010-PETITION UNDER RULE 137(10-9-2012).pdf

413-MUMNP-2010-REPLY TO EXAMINATION REPORT(10-9-2012).pdf

413-MUMNP-2010-REPLY TO EXAMINATION REPORT(6-3-2013).pdf

413-MUMNP-2010-REPLY TO HEARING(10-3-2014).pdf

413-MUMNP-2010-RUSSIAN DOCUMENT(10-9-2012).pdf

413-MUMNP-2010-US DOCUMENT(10-9-2012).pdf

abstract1.jpg

Drawings.PDF

Form-1.pdf

Form-3.pdf

Form-5.pdf