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...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
1997-05-01
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Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/2/5/80/ |