2011
DOI: 10.1016/j.carres.2011.03.025
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Structures of the novel diterpene glycosides from Stevia rebaudiana

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Cited by 68 publications
(54 citation statements)
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“…The 1 H NMR spectral data of 1 showed the presence of two methyl singlets at δ 1.12 and 1.40, two olefinic protons as singlets at δ 5.05 and 5.66 of an exocyclic double bond, nine sp3 methylene and two sp3 methine protons between δ 0.75 -2.67, characteristic for the ent-kaurane diterpenoids isolated earlier from the genus Stevia [12]- [15]. The basic skeleton of ent-kaurane diterpenoids was supported by the TOCSY studies which showed key correlations: H-1/H-2; H-2/H-3; H-5/H-6; H-6/H-7; H-9/H-11; H-11/H-12.…”
Section: Resultsmentioning
confidence: 99%
“…The 1 H NMR spectral data of 1 showed the presence of two methyl singlets at δ 1.12 and 1.40, two olefinic protons as singlets at δ 5.05 and 5.66 of an exocyclic double bond, nine sp3 methylene and two sp3 methine protons between δ 0.75 -2.67, characteristic for the ent-kaurane diterpenoids isolated earlier from the genus Stevia [12]- [15]. The basic skeleton of ent-kaurane diterpenoids was supported by the TOCSY studies which showed key correlations: H-1/H-2; H-2/H-3; H-5/H-6; H-6/H-7; H-9/H-11; H-11/H-12.…”
Section: Resultsmentioning
confidence: 99%
“…The most profound steviol glycosides are stevioside and rebaudioside A, which are present in high amounts [7][8][9][10][11][12][13][14][15][16][17].…”
Section: Steviol Glycosidesmentioning
confidence: 99%
“…Earlier phytochemical research has shown that the genus Bupleurum mainly accumulates saikosaponins [1][2]. As a part of our research to discover natural sweeteners, we have recently reported several diterpene glycosides from Stevia rebaudiana and Rubus suavissimus; triterpene glycosides from Siraitia grosvenorii; phenolic glycosides and sterols from R. suavissimus [3][4][5][6][7][8][9][10][11][12].…”
Section: Introductionmentioning
confidence: 99%