Planar Transition Structures in the Epoxidation of Alkenes. A DFT Study on the Reaction of Peroxyformic Acid with Norbornene Derivatives-Reference-Cited by-同舟云学术

Planar Transition Structures in the Epoxidation of Alkenes. A DFT Study on the Reaction of Peroxyformic Acid with Norbornene Derivatives

Published:2002-11-01 Issue:24 Volume:67 Page:8519-8527
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Freccero Mauro¹,Gandolfi Remo¹,Sarzi-Amadè Mirko¹,Rastelli Augusto¹

Affiliation:

1. Dipartimento di Chimica Organica, Università di Pavia, V.le Taramelli 10, 27100 Pavia, Italy, and Dipartimento di Chimica, Università di Modena, Via Campi 183, 41100 Modena, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo026141w

Reference45 articles.

1. High-Level Computational Study of the Stereoelectronic Effects of Substituents on Alkene Epoxidations with Peroxyformic Acid

2. A Computational Study of the Hydroxy-Group Directivity in the Peroxyformic Acid Epoxidation of the Chiral Allylic Alcohol (Z)-3-Methyl-3-penten-2-ol: Control of Threo Diastereoselectivity through Allylic Strain and Hydrogen Bonding

3. Nature of the Transition Structure for Alkene Epoxidation by Peroxyformic Acid, Dioxirane, and Dimethyldioxirane: A Comparison of B3LYP Density Functional Theory with Higher Computational Levels

4. Transition States of Epoxidations: Diradical Character, Spiro Geometries, Transition State Flexibility, and the Origins of Stereoselectivity

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