The preparation and electrocyclic ring-opening of cyclobutenes: Stereocontrolled approaches to substituted conjugated dienes and trienes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference51 articles.
1. The Conservation of Orbital Symmetry
2. Thermal electrocyclic ring-opening of cyclobutenes: stereoselective routes to functionalised conjugated (Z,E)- and (E,E)-2,4-dienals
3. Prediction and experimental verification of the stereoselective electrocyclization of 3-formylcyclobutene
4. Theory of stereoselection in conrotatory electrocyclic reactions of substituted cyclobutenes
5. Acid-base-controlled torquoselectivity: theoretical predictions of the stereochemical course of the electrocyclic reactions of cyclobutene-3-carboxylic acid and the conjugate base and acid
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