The synthesis of cholestane and furostan saponin analogues and the determination of sapogenin's absolute configuration at C-22

Steroids

Volumn 76, Issue 1-2, 2011, Pages 18-27

  Wang, Haixing ^a   Guo, Yanshen ^a   Guan, Yuyao ^a   Zhou, Liang ^a   Lei, Pingsheng ^a  

^a BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

Author keywords

Cholestane; Furostan; Glycosylation

Indexed keywords

(22,25) 3 BETA,22,26 TRIHYDROXY CHOLEST 5 ENE 16 ONE 22 O [O ALPHA RHAMNOPYRANOSYL (1 2) BETA GLUCOPYRANOSIDE]; (22,25) FUROST 5 ENE 3 BETA,22,26 TRIOL 22 O (ALPHA GLUCOPYRANOSIDE); (22,25) FUROST 5 ENE 3 BETA,22,26 TRIOL 22 O [O ALPHA RHAMNOPYRANOSYL (1 2) ALPHA GLUCOPYRANOSIDE]; (25) 3 BETA, 16 BETA,26 TRIHYDROXYCHOLEST 5 ENE 22 ONE 16 O [O ALPHA RHAMNOPYRANOSYL (1 2) BETA GLUCOPYRANOSIDE]; (25) 3 BETA,16 BETA,26 TRIHYDROXY CHOLEST 5 ENE 22 ONE 16 O [O ALPHA RHAMNOPYRANOSYL (1 2) ALPHA GLUCOPYRANOSIDE]; CHOLESTANE DERIVATIVE; DIOSGENIN; FUROSTAN SAPONIN; SAPONIN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CANCER CELL; CHIRALITY; CONTROLLED STUDY; CYTOTOXICITY; DRUG CONFORMATION; DRUG DETERMINATION; DRUG STRUCTURE; DRUG SYNTHESIS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

CHOLESTANES; MOLECULAR CONFORMATION; SAPOGENINS; SAPONINS; STEREOISOMERISM;

EID: 78650516089     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2010.07.011     Document Type: Article

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