Torquoselectivity in Cyclobutene Ring Openings and the Interatomic Interactions That Control Them
Author:
Affiliation:
1. Instituto de Química, Universidad Nacional Autónoma de México, Circuito exterior, Ciudad Universitaria Coyoacán, México, D.F., México 04510
Funder
Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.6b08771
Reference71 articles.
1. Remarkable, contrasteric, electrocyclic ring opening of a cyclobutene
2. Stereoselective substituent effects on conrotatory electrocyclic reactions of cyclobutenes
3. Electronic Control of Stereoselectivities of Electrocyclic Reactions of Cyclobutenes: A Triumph of Theory in the Prediction of Organic Reactions
4. Transition Structures of Thermally Allowed Disrotatory Electrocyclizations. The Prediction of Stereoselective Substituent Effects in Six-Electron Pericyclic Reactions
5. The Woodward−Hoffmann−De Puy Rule Revisited
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