ASYMMETRIC-SYNTHESIS OF 1-ARYL-1,2,3,4-TETRAHYDROISOQUINOLINES .1. ADDITION OF CHIRAL PHENYLACETALDEHYDE ACETALS TO ACYLIMINES

被引:14
作者
WUNSCH, B
NERDINGER, S
机构
[1] Institut für Pharmazie, Lebensmittelchemie der Universität München, D-80333 Munich
关键词
D O I
10.1016/0040-4039(95)01716-U
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The stereoselectivity in the addition of the enantiomerically pure (2-bromophenyl)acetaldehyde acetals 3a-g to the acylimines 4a,b is investigated. Based on this reaction a novel asymmetric synthesis for the 1-phenyl-tetrahydroisoquinoline 8 is elaborated.
引用
收藏
页码:8003 / 8006
页数:4
相关论文
共 24 条
[21]  
WUNSCH B, 1995, IN PRESS TETRAHEDRON
[22]   ASYMMETRIC REDUCTION OF CYCLIC IMINES WITH CHIRAL SODIUM ACYLOXYBOROHYDRIDES [J].
YAMADA, K ;
TAKEDA, M ;
IWAKUMA, T .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1983, (02) :265-270
[23]   A NOVEL ASYMMETRIC REDUCTION OF IMINES WITH CHIRAL SODIUM TRIACYLOXYBOROHYDRIDES [J].
YAMADA, K ;
TAKEDA, M ;
IWAKUMA, T .
TETRAHEDRON LETTERS, 1981, 22 (39) :3869-3872
[24]  
YAMATO M, 1990, TETRAHEDRON, V46, P5902