Nine-step enantioselective total synthesis of (-)-vincorine

Journal of the American Chemical Society

Volumn 135, Issue 17, 2013, Pages 6442-6445

  Horning, Benjamin D ^a   MacMillan, David W C ^a  

^a PRINCETON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DIELS-ALDER; ENANTIOSELECTIVE TOTAL SYNTHESIS; IMINIUM; KEY ELEMENTS; ORGANOCATALYTIC; RING SYSTEMS; STEREO-SELECTIVE; TOTAL SYNTHESIS;

ALKALOIDS; ENANTIOSELECTIVITY; METABOLITES; NITROGEN COMPOUNDS; SYNTHESIS (CHEMICAL);

CYCLIZATION;

ALKALOID DERIVATIVE; UNCLASSIFIED DRUG; VINCORINE;

ARTICLE; CATALYST; CYCLIZATION; DIELS ALDER REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; ELECTRON; ENANTIOSELECTIVITY; ISOMER; REACTION OPTIMIZATION; STEREOCHEMISTRY;

CYCLIZATION; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; STEREOISOMERISM; VINCA ALKALOIDS; X-RAY DIFFRACTION;

EID: 84877036747     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja402933s     Document Type: Article

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