The Pivotal Role of Oxyallyl Diradicals in Photo-Favorskii Rearrangements: Transient Spectroscopic and Computational Studies
Author:
Affiliation:
1. Department of Chemistry, University of Kansas, 1251 Wescoe Hall Drive, 5010 Malott Hall, Lawrence, Kansas 66045, United States
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja407588p
Reference46 articles.
1. Allene epoxidation. Isolation of a cyclopropanone
2. Thermal interconversion of a pair of diastereomeric cyclopropanones. An upper limit for a cyclopropanone-oxyallyl energy separation
3. Ring Opening of Bicyclo[n.1.0]alkanones to 2-Cycloalkanone-1,3-diyls. Why Does Oxyallyl Diradical Formation Require Less Energy from Bicyclo[3.1.0]hexan-6-ones than from Bicyclo[1.1.0]butan-2-ones?
4. Rearrangements of Allene Oxide, Oxyallyl, and Cyclopropanone
5. α-Halo Ketones. IV. The Isomeric α-Chloroketones Derived from 3-Heptanone
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