New insights about electronic mechanism of electrocyclic reactions: theoretical study about stereoselectivity in cyclobutenes-Reference-Cited by-同舟云学术

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New insights about electronic mechanism of electrocyclic reactions: theoretical study about stereoselectivity in cyclobutenes

Published:2021-04 Issue:4 Volume:7 Page:e06675
ISSN:2405-8440
Container-title:Heliyon
language:en
Short-container-title:Heliyon

Author:

Morales-Bayuelo Alejandro^ORCID,Sánchez-Márquez Jesús

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference58 articles.

1. Electronic control of stereoselectivities of electrocyclic reactions of cyclobutenes: a triumph of theory in the prediction of organic reactions;Dolbier;Acc. Chem. Res.,1996

2. Substituent effects on rates and stereoselectivities of conrotatory electrocyclic reactions of cyclobutenes. A theoretical study;Niwayama;J. Org. Chem.,1996

3. Theoretical predictions of torquoselectivity in pentadienyl cation electrocyclizations;Kallel;J. Org. Chem.,1989

4. Theoretical studies of the Nazarov cyclization 3. Torquoselectivity and hyperconjugation in the Nazarov cyclization. The effects of inner versus outer .beta.-methyl and .beta.-silyl groups;Smith;J. Org. Chem.,1993

5. Theoretical studies of the Nazarov cyclization. 2. The effect of .beta.-silyl and .beta.-methyl groups;Smith;J. Org. Chem.,1991

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1. A closer look to the bispericyclic transition structure leading to 4 + 2 and 2 + 4 cycloadducts in the endo dimerization of cyclopentadiene;International Journal of Quantum Chemistry;2023-12-23

2. An analysis of the torquoselectivity effect in a ring-opening reaction through Fermi–Dirac’s entropy: revealing the origin of the stereoselectivity.;Journal of Mathematical Chemistry;2023-09-23

3. Philicity scales using molecular quantum similarity and chemical reactivity indices within density functional theory;International Journal of Quantum Chemistry;2023-08-11

4. Local reactivity descriptors of the important atoms in chelotropic reactions provide insight into their global variants along the reaction path;International Journal of Quantum Chemistry;2023-03-29

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