Theoretical Predictions of Substituent Effects on the Thermal Electrocyclic Ring Openings of Cyclobutenones
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (7) , 2517-2522
- https://doi.org/10.1021/jo950899g
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- A potentially general regiospecific synthesis of substituted quinones from dimethyl squarateThe Journal of Organic Chemistry, 1992
- Annelation reactions of 4-alkynylcyclobutenones. Formation of methylenebenzofuransThe Journal of Organic Chemistry, 1991
- Synthesis of the bicyclo[3.2.0] ring systems from 4-allylcyclobutenones. Intramolecular ketene/alkene cycloadditionsThe Journal of Organic Chemistry, 1991
- Theoretical studies of the Nazarov cyclization. 2. The effect of .beta.-silyl and .beta.-methyl groupsThe Journal of Organic Chemistry, 1991
- An ab initio study of the cyclization and rearrangement of vinyl-, imidoyl-, and formylketeneThe Journal of Organic Chemistry, 1990
- Acid-base-controlled torquoselectivity: theoretical predictions of the stereochemical course of the electrocyclic reactions of cyclobutene-3-carboxylic acid and the conjugate base and acidThe Journal of Organic Chemistry, 1989
- Prediction and experimental verification of the stereoselective electrocyclization of 3-formylcyclobuteneThe Journal of Organic Chemistry, 1987
- Stereoselective substituent effects on conrotatory electrocyclic reactions of cyclobutenesJournal of the American Chemical Society, 1984
- Stereochemical selectivities in the electrocyclic valence isomerizations of cyclobutenones and 2,4-cyclohexadienonesJournal of the American Chemical Society, 1968
- The General Applicability of a Fixed Scale of Inductive Effects. II. Inductive Effects of Dipolar Substituents in the Reactivities of m- and p-Substituted Derivatives of Benzene1,2Journal of the American Chemical Society, 1958