Studies on the acid-catalyzed opening of non-rigid: acylcyclopropanes: a dramatic solvent effect. A route to the bicyclo[2.2.1]heptane ring system
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Six-membered rings via olefin participation in the opening of acylcyclopropanes
2. Aryl participation in concerted cyclization of cyclopropyl ketones
3. Olefin participation in the acid-catalyzed opening of acylcyclopropanes. III. Formation of the bicyclo[2.2.1]heptane system
4. Olefin participation in the acid-catalyzed opening of acylcyclopropanes. IV. Cyclization of 5-methyl-6--(-3-pentenyl)bicyclo(3.1.0)hexan-2-one.
5. A simple synthesis of (±)-cedrene and (±)-cedrol using a synchronous double annulation process
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3. Intramolecular donor–acceptor cyclopropane ring-opening cyclizations;Chem. Soc. Rev.;2014
4. Lewis Acid Catalyzed Formal Intramolecular [3+2] Cross-Cycloaddition of Cyclopropane 1,1-Diesters with Alkenes: General and Efficient Strategy for Construction of Bridged [n.2.1] Carbocyclic Skeletons;Angewandte Chemie International Edition;2013-01-10
5. Lewis Acid Catalyzed Formal Intramolecular [3+2] Cross-Cycloaddition of Cyclopropane 1,1-Diesters with Alkenes: General and Efficient Strategy for Construction of Bridged [n .2.1] Carbocyclic Skeletons;Angewandte Chemie;2013-01-10
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