Chiral N-substituted 4,5,6,7-tetrahydroindoles

被引：10

作者：

Grigg, R

Yoganathan, G

机构：

[1] School of Chemistry, Leeds University

来源：

TETRAHEDRON-ASYMMETRY | 1996年 / 7卷 / 01期

关键词：

D O I：

10.1016/0957-4166(95)00444-0

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

2-Formylmethylcyclohexanone reacts with alpha-amino esters in dry dichloromethane at room temperature to give homochiral N-substituted 4,5,6,7-tetrahydroindoles in good yield, No Pictet-Spengler products are observed with histidine or tryptophan esters.

引用

页码：273 / 276

页数：4

共 6 条

[1]

BACIOCCHI E, 1990, SYNLETT, P679

[2] RECENT ADVANCES IN CHEMISTRY OF PYRROLE [J].