The enantiospecific, stereospecific total synthesis of the ring-A oxygenated sarpagine indole alkaloids (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-Na-methylsarpagine, as well as the total synthesis of the Alstonia bisindole alkaloid macralstonidine

Journal of Organic Chemistry

Volumn 68, Issue 16, 2003, Pages 6279-6295

  Zhao, Shuo ^a   Liao, Xuebin ^a   Wang, Tao ^a   Flippen Anderson, Judith ^b,c   Cook, James M ^a  

^a UNIVERSITY OF WISCONSIN MILWAUKEE   (United States)

^b NAVAL RESEARCH LABORATORY   (United States)

^c RUTGERS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ORGANIC COMPOUNDS; SYNTHESIS (CHEMICAL);

ALKALOIDS;

STEREOCHEMISTRY;

10 METHOXYAFFINISINE; INDOLE ALKALOID; MACRALSTONIDINE; MAJVININE; N METHYLSARPAGINE; SARPAGINE; TRYPTOPHAN; UNCLASSIFIED DRUG;

ALSTONIA; ARTICLE; CHEMICAL REACTION; CHIRALITY; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; OXYGENATION; PLANT; STEREOSPECIFICITY;

ALSTONIA; CATALYSIS; CRYSTALLOGRAPHY, X-RAY; INDICATORS AND REAGENTS; INDOLE ALKALOIDS; INDOLES; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; MOLECULAR CONFORMATION; PALLADIUM; STEREOISOMERISM;

EID: 0041529903     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo030055u     Document Type: Article

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