FUNCTIONALIZED 2-AZABICYCLO[3.3.1]NONANES .13. THE FISCHER INDOLIZATION OF 2-AZABICYCLO[3.3.1]NONAN-7-ONES - A NEW ENTRY TO THE DASYCARPIDAN RING-SYSTEM

被引：20
作者：
BONJOCH, J
CASAMITJANA, N
GRACIA, J
UBEDA, MC
BOSCH, J
机构：
[1] Laboratory of Organic Chemistry, Faculty of Pharmacy, University of Barcelona
来源：
TETRAHEDRON LETTERS | 1990年 / 31卷 / 17期
关键词：
D O I：
10.1016/S0040-4039(00)97386-6
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The regloselectivity of the Fischer indole synthesis from 2-azabicyclo[3.3.1]nonan-7-ones 4b-d using three different acid catalysts is studied, an ethyl substituent at the 9-position promoting indolization upon the C-8 carbon. © 1990.
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页码：2449 / 2452
页数：4
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