SHORT FORMAL SYNTHESES OF INDOLE ALKALOIDS OF THE ULEINE AND STRYCHNOS GROUPS

被引：14

作者：

AMAT, M

SATHYANARAYANA, S

HADIDA, S

BOSCH, J

机构：

[1] Laboratory of Organic Chemistry, Faculty of Pharmacy, University of Barcelona

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 38期

关键词：

D O I：

10.1016/0040-4039(94)88242-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The formal synthesis of ulcine-type (dasycarpidone, dasycarpidol, uleine, and 17-hydroxy-16,17-dihydrouleine) and Strychnos alkaloids belonging to both the Strychnan (tubifoline, tubifolidine, and 19,20-dihydroakuammicine) and Aspidospermatan (tubotaiwine) skeletal types from 3-(2-pyridyl)indoles is described.

引用

页码：7123 / 7126

页数：4

共 14 条

[1] A NEW SYNTHETIC ENTRY TO PENTACYCLIC STRYCHNOS ALKALOIDS - TOTAL SYNTHESIS OF (+/-)-TUBIFOLIDINE, (+/-)-TUBIFOLINE, AND (+/-)-19,20-DIHYDROAKUAMMICINE
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[7] TOTAL SYNTHESIS OF THE STRYCHNOS ALKALOID TUBOTAIWINE
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[9] SYNTHESES OF (+)-DASYCARPIDONE, (+)-3-EPI-DASYCARPIDONE, (+)-ULEINE AND (+)-3-EPI-ULEINE
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[10] ALKALOID STUDIES .53. STRUCTURES OF 9 NEW ALKALOIDS FROM ASPIDOSPERMA DASYCARPON A DC
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