STUDIES ON THE SYNTHESIS OF PENTACYCLIC STRYCHNOS INDOLE ALKALOIDS - CLOSURE OF E-RING BY PUMMERER CYCLIZATION

被引：38

作者：

AMAT, M ^{[1
]}

BOSCH, J ^{[1
]}

机构：

[1] UNIV BARCELONA,FAC PHARM,ORGAN CHEM LAB,E-08028 BARCELONA,SPAIN

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1992年 / 57卷 / 21期

关键词：

D O I：

10.1021/jo00047a047

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[No abstract available]

引用

页码：5792 / 5796

页数：5

共 28 条

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[4] STUDIES ON THE SYNTHESIS OF STRYCHNOS INDOLE ALKALOIDS
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[6] METHODS FOR INDOLE ALKALOID SYNTHESIS - COMPATIBILITY OF THE 16-METHOXY SUBSTITUENT WITH THE INDOLE-2,3-QUINODIMETHANE STRATEGY TO ASPIDOSPERMA-TYPE INDOLE ALKALOIDS
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[7] THIOAMMONIUM IONS - AZASULFENYLATION REACTIONS
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[8] SYNTHESIS OF 5-ETHYL-11H-PYRIDO[3,4-A]CARBAZOLE BY 2 ROUTES AND CONVERSION OF ULEINE INTO 5-ETHYL-1,2,3,4-TETRAHYDRO-2-METHYL-11H-PYRIDO[3,4-A]CARBAZOLE
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[9] de Lucchi O, 2004, ORG REACTIONS, V40, P157
[10] SYNTHETIC APPLICATIONS OF "2-CYANO-1,2,3,6-TETRAHYDROPYRIDINES - IMPROVED SYNTHESIS OF THE FUNDAMENTAL TETRACYCLIC FRAMEWORK OF DASYCARPIDONE
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