High pressure -Lewis acid catalyzed diels-alder reactions of 3-methylcyclohex-2-en-1-one. A straightforward route to cis and Tras angularly methylated octalones.-Reference-Cited by-同舟云学术

High pressure -Lewis acid catalyzed diels-alder reactions of 3-methylcyclohex-2-en-1-one. A straightforward route to cis and Tras angularly methylated octalones.

Published:1991-10 Issue:44 Volume:32 Page:6445-6448
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Aben René W.M.,Minuti Lucio,Scheeren Hans W.,Taticchi Aldo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. Diels-Alder Reaction of 2-Methyl-2-cyclohexenone and Substituted Butadienes

2. Diels-Alder reactions involving cross-conjugated dienones. Effects of substitution on reactivity

3. Total synthesis of tetracyclic sesquiterpenoids: (±)-ishwarone

4. Diels-Alder reactions of cycloalkenones. 3. Effects of specific reaction parameters

5. Diels-Alder reactions of cycloalkenones. 15. Synthesis of cis- and trans-.DELTA.6-4a-methyl-1-octalones

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