CONSTRUCTION OF CONTIGUOUS QUATERNARY AND TERTIARY CARBON CENTERS VIA THE ASYMMETRIC MICHAEL REACTION

被引:26
作者
TOMIOKA, K [1 ]
YASUDA, K [1 ]
KOGA, K [1 ]
机构
[1] UNIV TOKYO,FAC PHARMACEUT SCI,BUNKYO KU,TOKYO 113,JAPAN
关键词
D O I
10.1039/c39870001345
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
引用
收藏
页码:1345 / 1346
页数:2
相关论文
共 13 条
[11]   A DIASTEREOSELECTIVE AND ENANTIOSELECTIVE MICHAEL ADDITION OF CHIRAL AMIDE ENOLATES TO PI,BETA-UNSATURATED ESTERS - A STEREOSELECTIVE SYNTHESIS OF (+)-DEHYDROIRIDODIOL AND (-)-ISODEHYDROIRIDODIOL [J].
YAMAGUCHI, M ;
HASEBE, K ;
TANAKA, S ;
MINAMI, T .
TETRAHEDRON LETTERS, 1986, 27 (08) :959-962
[12]   A HIGHLY STEREOSELECTIVE SYNTHESIS OF CARBOCYCLIC COMPOUNDS BY THE MICHAEL INDUCED INTRAMOLECULAR ALKYLATION - A STEREOCONTROL OF EXTRACYCLIC CHIRAL CENTERS [J].
YAMAGUCHI, M ;
TSUKAMOTO, M ;
HIRAO, I .
TETRAHEDRON LETTERS, 1985, 26 (14) :1723-1726
[13]   THE THREO-SELECTIVE REACTION OF BUT-2-ENYL ORGANOMETALLIC COMPOUNDS WITH ETHYLIDENEMALONATES AND RELATED-COMPOUNDS [J].
YAMAMOTO, Y ;
NISHII, S ;
MARUYAMA, K .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1985, (07) :386-388