An asymmetry induced azepine-ring formation through the ene reactions at the periphery of heterocyclic systems
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
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1. On-Demand Selection of the Reaction Path from Imino Diels-Alder to Ene-Type Cyclization: Synthesis of Epiminopyrimido[4,5-b]azepines;European Journal of Organic Chemistry;2013-11-19
2. [1,7]-Electrocyclization reactions in the synthesis of azepine derivatives;Chemistry of Heterocyclic Compounds;2013-04
3. ChemInform Abstract: An Asymmetry Induced Azepine-Ring Formation Through the Ene Reactions at the Periphery of Heterocyclic Systems.;ChemInform;2010-08-04
4. Bicyclic 6-6 Systems with One Bridgehead (Ring Junction) Nitrogen Atom: One Extra Heteroatom 1:0;Comprehensive Heterocyclic Chemistry III;2008
5. Competitive thermal ene reaction and Diels–Alder reactions of 2-[N-(alk-2-enyl)benzylamino]-3-vinylpyrido[1,2-a]pyrimidin-4(4H)-ones;Tetrahedron;2007-05
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