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DIASTEREOSELECTIVITY IN NUCLEOPHILIC-ADDITION REACTIONS TO (ALPHA-BETA-DIALKOXYACYL)SILANES - AN OPERATIONALLY USEFUL ROUTE TO OPTICALLY-ACTIVE 1,2,3-SYN-TRIOLS
被引:37
作者
:
CIRILLO, PF
论文数:
0
引用数:
0
h-index:
0
机构:
BOSTON UNIV,METCALF CTR SCI & ENGN,DEPT CHEM,BOSTON,MA 02215
BOSTON UNIV,METCALF CTR SCI & ENGN,DEPT CHEM,BOSTON,MA 02215
CIRILLO, PF
[
1
]
PANEK, JS
论文数:
0
引用数:
0
h-index:
0
机构:
BOSTON UNIV,METCALF CTR SCI & ENGN,DEPT CHEM,BOSTON,MA 02215
BOSTON UNIV,METCALF CTR SCI & ENGN,DEPT CHEM,BOSTON,MA 02215
PANEK, JS
[
1
]
机构
:
[1]
BOSTON UNIV,METCALF CTR SCI & ENGN,DEPT CHEM,BOSTON,MA 02215
来源
:
JOURNAL OF ORGANIC CHEMISTRY
|
1990年
/ 55卷
/ 25期
关键词
:
D O I
:
10.1021/jo00312a005
中图分类号
:
O62 [有机化学];
学科分类号
:
070303 ;
081704 ;
摘要
:
: [syn-α-Alkoxy-β-(silyloxy)acyl]silanes 3 undergo chelation-controlled nucleophilic addition reactions to produce Cram-type addition products (1,2,3-syn-triol derivatives) 4 with useful levels of diastereoselectivity. © 1990, American Chemical Society. All rights reserved.
引用
收藏
页码:6071 / 6073
页数:3
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