General approach for the synthesis of 12-methoxy-substituted sarpagine indole alkaloids including (-)-12-methoxy-Nb-methylvoachalotine, (+)-12-methoxy-Na-methylvellosimine, (+)-12-methoxyaffinisine, and (-)-fuchsiaefoline

Journal of Organic Chemistry

Volumn 71, Issue 1, 2006, Pages 251-259

  Zhou, Hao ^a   Liao, Xuebin ^a   Yin, Wenyuan ^a   Ma, Jun ^a   Cook, James M ^a  

^a UNIVERSITY OF WISCONSIN MILWAUKEE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; ETHERS; FORMALDEHYDE; OXIDATION; SYNTHESIS (CHEMICAL);

AXIAL POSITION; ETHYL ESTER; HETEROANNULATION;

ESTERS;

12 METHOXY N METHYLVELLOSIMINE; 12 METHOXY N METHYLVOACHALOTINE; 12 METHOXYAFFINISINE; 7 METHOXYTRYPTOPHAN ETHYL ESTER; FUCHSIAEFOLINE; INDOLE ALKALOID; SARPAGINE; TRYPTOPHAN; UNCLASSIFIED DRUG;

ANNULATION REACTION; ARTICLE; CHEMICAL REACTION KINETICS; CHIRALITY; CROSS COUPLING REACTION; CYCLIZATION; DEPROTECTION REACTION; ENANTIOMER; OXIDATION KINETICS; PICTET SPENGLER REACTION; PRODUCT RECOVERY; REACTION ANALYSIS; SYNTHESIS;

ETHERS, CYCLIC; INDOLE ALKALOIDS; KETONES; MOLECULAR STRUCTURE; STEREOISOMERISM; TRYPTOPHAN;

EID: 31144432900     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo052081t     Document Type: Article

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