Thermolyses of O-Phenyl Oxime Ethers. A New Source of Iminyl Radicals and a New Source of Aryloxyl Radicals-Reference-Cited by-同舟云学术

Thermolyses of O-Phenyl Oxime Ethers. A New Source of Iminyl Radicals and a New Source of Aryloxyl Radicals

Published:2004-04-01 Issue:9 Volume:69 Page:3112-3120
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Blake Jessie A.¹,Pratt Derek A.¹,Lin Shuqiong¹,Walton John C.¹,Mulder Peter¹,Ingold K. U.¹

Affiliation:

1. National Research Council, Ottawa, Ontario K1A 0R6, Canada, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, University of St. Andrews, St. Andrews KY16 9ST, U.K., and Leiden Institute of Chemistry, Leiden University, 2300 RA Leiden, The Netherlands

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo049927y

Reference32 articles.

1. Thermal decomposition of O-benzyl ketoximes; role of reverse radical disproportionation

2. Tautomerism in 1,5-dianilino-4,8-naphthoquinones

3. The formation of an enantiomerically pure product of free radical coupling. The chemistry of diphenylcarbene in polycrystalline S-(+)-2-butanol

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