The torquoselectivity of electrocyclic reactions of 3-donor-3-acceptor-substituted cyclobutenes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Stereoselective substituent effects on conrotatory electrocyclic reactions of cyclobutenes
2. Theory of stereoselection in conrotatory electrocyclic reactions of substituted cyclobutenes
3. Prediction and experimental verification of the stereoselective electrocyclization of 3-formylcyclobutene
4. Competition between ester and formyl groups for control of torquoselectivity in cyclobutene electrocyclic reactions
5. Lewis acid reversal of the torquoselectivity of the electrocyclic ring opening of 3-acetylcyclobutene
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1. Torquoselectivity of Conrotatory Ring Opening in 3-Substituted Cyclobutenes;Steric and Stereoelectronic Effects in Organic Chemistry;2021
2. Distinguishing and quantifying the torquoselectivity in competitive ring-opening reactions using the stress tensor and QTAIM;Journal of Computational Chemistry;2016-10-06
3. Competitive and Cooperative Torquoselectivity in the thermal ring opening of cyclobutene: A density functional insight;Journal of Chemical Sciences;2015-09
4. Analyzing torquoselectivity in electrocyclic ring opening reactions of trans-3,4-dimethylcyclobutene and 3-formylcyclobutene through electronic structure principles;Physical Chemistry Chemical Physics;2015
5. Progress in the Synthesis and Transformations of Alkylidenecyclopropanes and Alkylidenecyclobutanes;Chemical Reviews;2014-06-13
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