SYNTHESIS OF ACYLSILANES FROM AMIDES AND ESTERS, AND THE SELECTIVE OXIDATION OF ALPHA-SILYL ALCOHOLS TO ALDEHYDES
被引:48
作者:
FLEMING, I
论文数: 0引用数: 0
h-index: 0
机构:University Chemical Laboratory, Cambridge CB2 1EW, Lensfield Road
FLEMING, I
GHOSH, U
论文数: 0引用数: 0
h-index: 0
机构:University Chemical Laboratory, Cambridge CB2 1EW, Lensfield Road
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.