Nucleophilic Attack of Siloxycarbenes on Carbonyl Groups. The Formation of Oxiranes
作者:
A. G. Brook,
Ronald Pearce,
J. B. Pierce,
期刊:
Canadian Journal of Chemistry
(NRC Available online 1971)
卷期:
Volume 49,
issue 10
页码: 1622-1628
ISSN:0008-4042
年代: 1971
DOI:10.1139/v71-265
出版商: NRC Research Press
数据来源: NRC
摘要:
Siloxycarbenes, formed by the photolysis of dimethyl- or diphenylsilacyclohexanone have been trapped as oxiranes or as the ring-opened hydrolysis products of oxiranes, with simple aldehydes and ketones such as acetaldehyde, or cyclohexanone. The reactions are interpreted as arising from the nucleophilic attack of the siloxycarbene on the carbonyl group. The structures of the oxiranes and their hydrolysis products have been established.
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