The Intramolecular Radical Cation Induced Diels-Alder Reaction in the Diene - Diene Format

The Intramolecular Radical Cation Induced Diels-Alder Reaction in the Diene - Diene Format

Two 1,3,8,10-undecatetraenes were synthesized to test the viability of the intramolecular radical cation induced Diels-Alder reaction in the diene - diene format. Cyclization was successful only for the substituted tetraene with the lower oxidation potential. The major hexahydroindene product posses...

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Bibliographic Details
Main Authors: Paul G. Gassman, David B. Gorman, David B. Rusterholz
Format: Article
Language:English
Published: MDPI AG 1997-05-01
Series:Molecules
Subjects:
Radical cation
Diels-Alder reaction
intramolecular cyclization
Online Access:http://www.mdpi.com/1420-3049/2/5/80/

Internet

http://www.mdpi.com/1420-3049/2/5/80/

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