Conjugate hydrocyanation of 17-acetyl-11-carbomethoxygona-1,3,5(10),13(17)-tetraenes

Steroids

Volumn 72, Issue 3, 2007, Pages 297-304

  Pellissier, Hélène ^a   Michellys, Pierre Yves ^b   Santelli, Maurice ^a  

^a AIX MARSEILLE UNIVERSITY   (France)

^b GENOMICS INSTITUTE OF THE NOVARTIS RESEARCH FOUNDATION   (United States)

Author keywords

C 13 substituted steroids; Cyanation; Functionalization of steroids; Unnatural steroids

Indexed keywords

17 ACETYL 11 CARBOMETHOXYGONA 1,3,5(10),13(17) TETRAENE; ALUMINUM DERIVATIVE; CYANIDE; DIETHYLALUMINUM CYANIDE; HYDROXYL GROUP; STEROID; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CONJUGATE; HYDROCYANATION; NAGARA REACTION; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION; STEREOCHEMISTRY; TRANS ISOMER;

ACETYLATION; CYANATES; GONANES; HYDROGEN CYANIDE; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; METHYLATION; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; STEROIDS; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 33847053272     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2006.11.022     Document Type: Article

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