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A FACILE ASYMMETRIC-SYNTHESIS OF BETA-SUBSTITUTED ALKANOIC ACID THE HIGHLY STEREOSELECTIVE MICHAEL ADDITION OF GRIGNARD-REAGENTS TO ALPHA,BETA-UNSATURATED CARBOXYLIC AMIDES DERIVED FROM L-EPHEDRINE
被引:84
|
作者
:
MUKAIYAMA, T
论文数:
0
引用数:
0
h-index:
0
MUKAIYAMA, T
IWASAWA, N
论文数:
0
引用数:
0
h-index:
0
IWASAWA, N
机构
:
来源
:
CHEMISTRY LETTERS
|
1981年
/ 07期
关键词
:
D O I
:
10.1246/cl.1981.913
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
引用
收藏
页码:913 / 916
页数:4
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CHEMICAL & PHARMACEUTICAL BULLETIN,
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[2]
HIGHLY STEREOSELECTIVE SYNTHESIS OF ALPHA,BETA-UNSATURATED KETONES BY CECL3 MEDIATED ADDITION OF GRIGNARD-REAGENTS TO BETA-ENAMINO KETONES
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[3]
ASYMMETRIC SYNTHESES USING TERT-LEUCINE .1. ASYMMETRIC SYNTHESIS OF BETA-SUBSTITUTED ALDEHYDES VIA 1,4-ADDITION OF GRIGNARD-REAGENTS TO CHIRAL ALPHA,BETA-UNSATURATED ALDIMINES
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[10]
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