Concerted and Stepwise Dissociative Electron Transfers. Oxidability of the Leaving Group and Strength of the Breaking Bond as Mechanism and Reactivity Governing Factors Illustrated by the Electrochemical Reduction of α-Substituted Acetophenones-Reference-Cited by-同舟云学术

Concerted and Stepwise Dissociative Electron Transfers. Oxidability of the Leaving Group and Strength of the Breaking Bond as Mechanism and Reactivity Governing Factors Illustrated by the Electrochemical Reduction of α-Substituted Acetophenones

Published:1997-03-01 Issue:10 Volume:119 Page:2420-2429
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Andrieux Claude P.¹,Savéant Jean-Michel¹,Tallec André¹,Tardivel Robert¹,Tardy Caroline¹

Affiliation:

1. Contribution from the Laboratoire d'Electrochimie Moléculaire de l'Université Denis Diderot, Unité Associée au CNRS No 438, 2 place Jussieu, 75251 Paris Cedex 05, France, and the Laboratoire d'Electrochimie de l'Université de Rennes, Unité Associée au CNRS No 439, Campus de Beaulieu, 35042, Rennes Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja963674b

Reference46 articles.

1. (a) Savéant, J.M. Single Electron Transfer and Nucleophilic Substitution inAdvances in Physical Organic Chemistry; Bethel, D., Ed.; Academic Press: New York, 1990; Vol. 26, pp 1−130.

2. Electron transfer, bond breaking, and bond formation

3. Mechanisms and reactivity in electron transfer induced aromatic nucleophilic substitution. Recent advances.

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