Chiral ligands derived from Abrine .3. Asymmetric Pictet-Spengler reaction of Abrine methyl ester and synthesis of chiral 1,2,3,4-tetrahydro-beta-carbolines as promoters in addition of diethylzinc toward aromatic aldehydes

被引:26
作者
Dai, WM [1 ]
Zhu, HJ [1 ]
Hao, XJ [1 ]
机构
[1] CHINESE ACAD SCI,KUNMING INST BOT,KUNMING 650204,YUNNAN,PEOPLES R CHINA
关键词
D O I
10.1016/0040-4039(96)01290-7
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Asymmetric Pictet-Spengler reaction of a number of aldehydes with Abrine methyl ester (1) was performed at room temperature to furnish mainly 3 and high ee was obtained in enantioselective addition of Et(2)Zn with PhCHO catalyzed by chiral 1,2,3,4-tetrahydro-beta-carboline derivatives 5 synthesized from 3. Copyright (C) 1996 Elsevier Science Ltd
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页码:5971 / 5974
页数:4
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[41]   A SUCCESSFUL ACID-PROMOTED ASYMMETRIC PICTET-SPENGLER REACTION OF N-A-BOC PROTECTED TRYPTOPHANS - EFFECT OF THE BOC GROUP ON REACTIVITY AND STEREOSELECTIVITY [J].
ZHANG, PW ;
COOK, JM .
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