Competition of Mechanisms in the Photochemical Cleavage of the C−X Bond of Aryl-Substituted Vinyl Halides-Reference-Cited by-同舟云学术

Competition of Mechanisms in the Photochemical Cleavage of the C−X Bond of Aryl-Substituted Vinyl Halides

Published:1998-11-24 Issue:25 Volume:63 Page:9292-9299
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Galli Carlo¹,Gentili Patrizia¹,Guarnieri Alessandra¹,Kobayashi Shinjiro¹,Zvi Rappoport ¹

Affiliation:

1. Dipartimento di Chimica, Università “La Sapienza”, 00185 Roma, Italy, Institute for Fundamental Research of Organic Chemistry, Kyushu University, Fukuoka 812, Japan, and Department of Organic Chemistry, The Hebrew University, Jerusalem 91904, Israel

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo981164p

Reference66 articles.

1. Photobehavior of alkyl halides in solution: radical, carbocation, and carbene intermediates

2. Photoreactivity of some .alpha.-arylvinyl bromides in acetic acid. Selectivity toward bromide versus acetate ions as a mechanistic probe

3. Photochemical Formation and Electrophilic Reactivities of Vinyl Cations. Influence of Substituents, Anionic Leaving Groups, Solvents, and Excitation Wavelength on Photoheterolysis and Photohomolysis of 1-(p-R-Phenyl)-2-(2,2'-biphenyldiyl)vinyl Halides

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