Cyclobutane formation in the 2π + 2π cycloaddition of allyl and related cations to unactivated olefins. Evidence for the second step in the proposed mechanism of the ionic diels-alder reaction.-Reference-Cited by-同舟云学术

Cyclobutane formation in the 2π + 2π cycloaddition of allyl and related cations to unactivated olefins. Evidence for the second step in the proposed mechanism of the ionic diels-alder reaction.

Published:1992-01 Issue:2 Volume:33 Page:157-160
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Gassman Paul G.,Lottes Andrew C.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Acid-catalyzed intramolecular "Diels-Alder" reactions. The cycloaddition of allyl cations to 1,3-dienes

2. Distinction between aminium cation radical and protic acid catalyzed Diels-Alder reactions

3. Control of regiospecificity in ionic Diels-Alder reactions. The use of allylic alcohols and allylic ethers as precursors of dienophilic allyl cations

4. Acrolein acetals as allyl cation precursors in the ionic Diels-Alder reaction

5. The low-temperature, ionic Diels-Alder addition of vinyl ortho esters to 1,3-dienes

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