1995年9月
ENE PREFERENCE IN THE REACTION OF ALLENYLMETHYLSILANES WITH HETERO-DOUBLE BONDS MEDIATED BY A LEWIS-ACID
JOURNAL OF ORGANOMETALLIC CHEMISTRY
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- ,
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- ,
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- 巻
- 499
- 号
- 1-2
- 開始ページ
- 155
- 終了ページ
- 157
- 記述言語
- 英語
- 掲載種別
- 研究論文（学術雑誌）
- DOI
- 10.1016/0022-328X(95)00306-B
- 出版者・発行元
- ELSEVIER SCIENCE SA LAUSANNE
Methylthio- and methoxy-substituted allenylmethylsilanes, a kind of allylsilanes, undergo the ene-type reaction, not the usual allylsilane-type reaction accompanying by desilylation, with carbonyl and azo compounds mediated by a Lewis acid. The corresponding 1-silyl-substituted functionalized 1,3-dienes are obtained in good yields.
- リンク情報
- ID情報
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- DOI : 10.1016/0022-328X(95)00306-B
- ISSN : 0022-328X
- Web of Science ID : WOS:A1995RR62400022