1998年
A facile preparation and cyclopropanation of 1-alkenylsilanols
Bulletin of the Chemical Society of Japan
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- 巻
- 71
- 号
- 10
- 開始ページ
- 2409
- 終了ページ
- 2417
- 記述言語
- 英語
- 掲載種別
- DOI
- 10.1246/bcsj.71.2409
- 出版者・発行元
- The Chemical Society of Japan
Alkenylsilanols are prepared by the reaction of hexamethyltrisiloxane (D3) with alkenyllithiums or alternatively by the reaction of cyclic siloxanes substituted by an alkenyl group with organolithiums and transformed to the corresponding cyclopropylsilanols using diiodomethane and diethylzinc. Lithium alkenylsilanolates, primary products of the preparation, also undergo cyclopropanation. As in the case of allylic alcohols, the silanol functionality is found to enhance the rate of cyclopropanation compared with that of alkenyltrialkylsilane or alkoxydialkylsilane. The obtained cyclopropylsilanols are further converted into the corresponding cyclopropanols by the Tamao oxidation.
- リンク情報
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- DOI
- https://doi.org/10.1246/bcsj.71.2409
- CiNii Articles
- http://ci.nii.ac.jp/naid/130004149930
- URL
- http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000076858600018&KeyUID=WOS:000076858600018
- URL
- http://orcid.org/0000-0002-1163-264X
- ID情報
-
- DOI : 10.1246/bcsj.71.2409
- ISSN : 0009-2673
- CiNii Articles ID : 130004149930