Diels - Alder reaction - Aromatization approach toward functionalized ring C allocolchicinoids. Enantioselective total synthesis of (-)-7S-allocolchicine

Journal of Organic Chemistry

Volumn 68, Issue 15, 2003, Pages 5826-5831

  Vorogushin, Andrei V ^a,b   Predeus, Alexander V ^a   Wulff, William D ^a   Hansen, Hans Jürgen ^b  

^a MICHIGAN STATE UNIVERSITY   (United States)

^b UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEXATION; ISOMERS; KETONES; NUCLEAR MAGNETIC RESONANCE; REDUCTION; SOLVENTS; STEREOCHEMISTRY; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

STEREOSELECTIVITY;

AROMATIZATION;

ALLOCOLCHICINE; ALLOCOLCHICINOID DERIVATIVE; ANNULENE DERIVATIVE; BENZENE DERIVATIVE; CARBENE; COLCHICINE; KETONE; UNCLASSIFIED DRUG; ZINC DERIVATIVE;

AROMATIZATION; ARTICLE; DIELS ALDER REACTION; ENANTIOSELECTIVITY; MITOSIS; MITSUNOBU REACTION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REDUCTION; STEREOCHEMISTRY; SYNTHESIS;

COLCHICINE; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 0038711432     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo034420t     Document Type: Article

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