SYNTHESIS OF ACYLSILANES FROM AMIDES AND ESTERS, AND THE SELECTIVE OXIDATION OF ALPHA-SILYL ALCOHOLS TO ALDEHYDES

被引:48
作者
FLEMING, I
GHOSH, U
机构
[1] University Chemical Laboratory, Cambridge CB2 1EW, Lensfield Road
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1994年 / 03期
关键词
D O I
10.1039/p19940000257
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The acylsilanes 2 can easily be made directly from the dimethylamides 3 by treatment with phenyldimethylsilyllithium. They can also be made in two steps from the esters 4 using 2 equiv. of phenyldimethylsilyllithium followed by oxidation of the disilyl alcohols 5 with PDC. The disilyl alcohols 5 can be used as intermediates in the conversion of esters into aldehydes without recourse to hydride reagents, by monodesilylation, using a Brook rearrangement. followed by oxidation and selective removal of the silyl group, using chromium trioxide in DMSO.
引用
收藏
页码:257 / 262
页数:6
相关论文
共 35 条