Enantiospecific total synthesis of the important biogenetic intermediates along the ajmaline pathway, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epivellosimine and Macusine A

Journal of Organic Chemistry

Volumn 75, Issue 10, 2010, Pages 3339-3349

  Yin, Wenyuan ^a   Kabir, M Shahjahan ^a   Wang, Zhijian ^a   Rallapalli, Sundari K ^a   Ma, Jun ^a   Cook, James M ^a  

^a UNIVERSITY OF WISCONSIN MILWAUKEE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AXIAL POSITIONS; CHIRAL AUXILIARIES; CROSS COUPLING REACTIONS; CROSS-COUPLINGS; DEPROTECTION; DIASTEREO-SELECTIVITY; DIECKMANN CYCLIZATION; ENANTIOSPECIFIC; ENOLATES; HYDROXYMETHYL GROUPS; METHYL ESTERS; NEW PROCESS; OXIDATIVE CYCLIZATION; PICTET-SPENGLER REACTIONS; REACTION VESSEL; REDUCTIVE CLEAVAGE; STARTING MATERIALS; STEREOSPECIFIC SYNTHESIS; TOTAL SYNTHESIS;

ALDEHYDES; AMINO ACIDS; BIOCHEMISTRY; COMPLEXATION; ESTERIFICATION; ESTERS; METHANOL; PALLADIUM; REACTION INTERMEDIATES; SYNTHESIS (CHEMICAL);

CYCLIZATION;

16 EPIVELLOSIMINE; AJMALINE; ALDEHYDE DERIVATIVE; ALKALOID; MACUSINE A; PALLADIUM; POLYNEURIDINE; SPERMINE DERIVATIVE; TRYPTOPHAN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CROSS COUPLING REACTION; CYCLIZATION; DEPROTECTION REACTION; STEREOCHEMISTRY; STEREOSPECIFICITY; SYNTHESIS;

AJMALINE; ALDEHYDES; INDOLE ALKALOIDS; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 77952515861     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo100279w     Document Type: Article

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