REDUCTION AND N-ALKYLATION OF ALPHA-METHYLENE-INDOLINES WITH SODIUM CYANOBOROHYDRIDE IN CARBOXYLIC-ACIDS

被引：1
|
作者：
BALOGH, ER [1 ]
ZSADON, B [1 ]
CSAMPAI, A [1 ]
PAL, R [1 ]
机构：
[1] HUNGARIAN OIL & GAS CO,DIV DEV & MKT,H-2443 SZAZHALOMBATTA,HUNGARY
来源：
SYNTHETIC COMMUNICATIONS | 1994年 / 24卷 / 05期
关键词：
D O I：
10.1080/00397919408012649
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The reaction of alpha-methylene-indolines with NaCNBH3 in carboxylic acids at room temperature can yield either 2beta,3beta-dihydro-indolines or their N-alkyl derivatives as main products with high selectivity, depending mainly on the carboxylic acid and on the reaction time when using a large excess of NaCNBH3.
引用
收藏
页码：701 / 707
页数：7
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