Hydrogen Atom Abstraction Selectivity in the Reactions of Alkylamines with the Benzyloxyl and Cumyloxyl Radicals. The Importance of Structure and of Substrate Radical Hydrogen Bonding-Reference-Cited by-同舟云学术

Hydrogen Atom Abstraction Selectivity in the Reactions of Alkylamines with the Benzyloxyl and Cumyloxyl Radicals. The Importance of Structure and of Substrate Radical Hydrogen Bonding

Published:2011-09-22 Issue:41 Volume:133 Page:16625-16634
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Salamone Michela¹,DiLabio Gino A.²³,Bietti Massimo¹

Affiliation:

1. Dipartimento di Scienze e Tecnologie Chimiche, Università “Tor Vergata”, Via della Ricerca Scientifica, 1 I-00133 Rome, Italy

2. National Institute for Nanotechnology, National Research Council of Canada, 11421 Saskatchewan Drive, Edmonton, Alberta, Canada T6G 2M9

3. Department of Physics, University of Alberta, Edmonton, Alberta, Canada T6G 2E1

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja206890y

Reference121 articles.

1. Product and Mechanistic Analysis of the Reactivity of a C6-Pyrimidine Radical in RNA

2. Interaction between Radicals Derived from Two Di-t-Alkyl Peroxides with Some Monomers and Polymers

3. Chemical Methods To Evaluate Antioxidant Ability

4. Free radical intermediates in the inhibition of the autoxidation reaction

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