Synthesis of Sterically Hindered Bicyclo[2.2.2]octanes by Lewis Acid Catalyzed Reaction of 2-(Trimethylsiloxy)-1,3-cyclohexadienes with 4-Methyl-3-penten-2-one-Reference-Cited by-同舟云学术

Synthesis of Sterically Hindered Bicyclo[2.2.2]octanes by Lewis Acid Catalyzed Reaction of 2-(Trimethylsiloxy)-1,3-cyclohexadienes with 4-Methyl-3-penten-2-one

Published:1987-06 Issue:6 Volume:60 Page:2259-2260
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Asaoka Morio,Ishibashi Keiji,Takahashi Wataru,Takei Hisashi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/60/6/60_6_2259/_pdf

Reference11 articles.

1. Total synthesis of (±)-eremolactone

2. Structure of 9-acetyl-4,8,8-trimethyltricyclo[5.2.2.01,5]undecan-6-ol

3. The synthesis of bicyclo[2.2.2]octan-2-ones by sequential michael reactions

4. Total synthesis of (.+-.)-seychellene. Use of silyloxydienes in synthesis

5. Studies with Bicyclo[2,2,2]octenes. VIII. Synthesis of the Tricyclo[5,2,2,01,5]-undecane skeleton related to eremolactone

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