Highly regioselective diels-alder reactions of 2-trimethylsilylmethyl- 1,3-butadiene catalyzed by a lewis acid and applications to syntheses of terpenes-Reference-Cited by-同舟云学术

Highly regioselective diels-alder reactions of 2-trimethylsilylmethyl- 1,3-butadiene catalyzed by a lewis acid and applications to syntheses of terpenes

Published:1982-01 Issue:5 Volume:23 Page:551-554
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Hosomi Akira,Iguchi Hirokazu,Sasaki Jun-ichi,Sakurai Hideki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. 2-trimethylsilylmethyl-1,3-butadiene as a novel reagent for isoprenylation. New access to ipsenol and ipsdienol, pheromones of Ips paraconfusus

2. Highly regioselective diels-alder reactions of 2-trimethylsilylmethyl- and 2-trimethylstannylmethyl-1,3-butadiene

3. Isoprene synthons. Silicon- and tin-mediated terpene synthesis

4. Catalytic Actions of Aluminum Chloride on the Isoprene—Methyl Acrylate Diels-Alder Reaction

5. Lewis acid catalysis of Diels-Alder reactions

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