The regioselectivity of [6+4] cycloadditions of dienamines to fulvenes.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. The [6 + 4] cycloadditions of diethylaminobutadiene to fulvenes. A new synthesis of azulenes
2. D. Mukherjee, L.C. Dunn, and K.N. Houk, submitted for publication.
3. Generalized frontier orbitals of alkenes and dienes. Regioselectivity in Diels-Alder reactions
4. Frontier molecular orbital theory of cycloaddition reactions
5. A frontier molecular orbital treatment of fulvene cycloadditions
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1. An overview of the cycloaddition chemistry of fulvenes and emerging applications;Beilstein Journal of Organic Chemistry;2019-09-06
2. Cycloaddition Reactions: Why Is It So Challenging To Move from Six to Ten Electrons?;Angewandte Chemie International Edition;2017-06-27
3. Cycloadditionen: Warum ist der Übergang von sechs zu zehn Elektronen so schwer?;Angewandte Chemie;2017-06-27
4. [m+n(+…)] Cycloaddition;Comprehensive Organic Name Reactions and Reagents;2010-09-15
5. A Cope Rearrangement-Based Route to Hexahydroazulenes;Organic Letters;2010-06-29
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