Tetra-glucopyranosyl Diterpene ent-Kaur-16-en-19-oic Acid and ent-13(S)-Hydroxyatisenoic Acid Derivatives from a Commercial Extract of Stevia rebaudiana (Bertoni) Bertoni.

and its diterpene glycosides are one of the main focuses of food companies interested in developing novel zero calorie sugar substitutes since the recognition of steviol glycosides as Generally Recognized as Safe (GRAS) by the United States Food and Drug Administration. Rebaudioside A, one of the major steviol glycosides of the leaves is more than 200 times sweeter than sucrose. However, its lingering aftertaste makes it less attractive as a table-top sweetener, despite its human health benefits. Herein, we report the purification of two novel tetra-glucopyranosyl diterpene glycosides and (rebaudioside A isomers) from a commercial leaf extract compounds, their saponification products compounds and , together with three known compounds isolated in gram quantities. Compound was determined to be 13-[(2--β-d-glucopyranosyl6--β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]-kaur-16-en-19-oic acid-β-d-glucopyranosy ester (rebaudioside Z), whereas compound was found to be 13-[(2--β-d-glucopyranosyl3--β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]-hydroxyatis-16-en-19-oic acid -β-d-glucopyranosy ester. Two new tetracyclic derivatives with no sugar at position C-19 were prepared from rebaudiosides and under mild alkaline hydrolysis to afford compounds 13-[(2--β-d-glucopyranosyl6--β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]-kaur-16-en-19-oic acid (rebaudioside Z₁) and 13-[(2--β-d-glucopyranosyl3--β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]-hydroxyatis-16-en-19-oic acid. Three known compounds were purified in gram quantities and identified as rebaudiosides A (), H () and J (). Chemical structures were unambiguously elucidated using different approaches, namely HRESIMS, HRESI-MS/MS, and 1D-and 2D-NMR spectroscopic data. Additionally, a high-quality crystal of iso-stevioside was grown in methanol and its structure confirmed by X-ray diffraction.