Efficient strategy for the synthesis of stereopentad subunits of scytophycin, Rifamycin S, and discodermolide

Organic Letters

Volumn 3, Issue 25, 2001, Pages 3995-3998

  Bouzbouz, S ^a   Cossy, J ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALKANE; ANTINEOPLASTIC AGENT; CARBAMIC ACID DERIVATIVE; DISCODERMOLIDE; LACTONE; PYRAN DERIVATIVE; PYRONE DERIVATIVE; RIFAMYCIN; RIFAMYCIN S; SCYTOPHYCIN A;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; STEREOISOMERISM; SYNTHESIS;

ALDEHYDES; ALKANES; ANTINEOPLASTIC AGENTS; CARBAMATES; LACTONES; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; PYRANS; PYRONES; RIFAMYCINS; STEREOISOMERISM;

EID: 0035856964     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016250h     Document Type: Article

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