Density Functional Theory Study of Hydrogen Atom Abstraction from a Series of para-Substituted Phenols: Why is the Hammett σp+ Constant Able to Represent Radical Reaction Rates?-Reference-Cited by-同舟云学术

Density Functional Theory Study of Hydrogen Atom Abstraction from a Series of para-Substituted Phenols: Why is the Hammett σp+ Constant Able to Represent Radical Reaction Rates?

Published:2011-05-02 Issue:11 Volume:76 Page:4564-4570
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yoshida Tatsusada¹,Hirozumi Koji¹,Harada Masataka¹,Hitaoka Seiji¹,Chuman Hiroshi¹

Affiliation:

1. Institute of Health Biosciences, The University of Tokushima Graduate School, 1-78 Shomachi, Tokushima 770-8505, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo200450p

Reference72 articles.

1. Comparative QSAR: Radical Reactions of Benzene Derivatives in Chemistry and Biology

2. Phenol toxicity in leukemia cells: a radical process?

3. Molecular orbital parameters and comparative QSAR in the analysis of phenol toxicity to leukemia cells

4. Toxicology of benzyl alcohols: a QSAR analysis

5. Comparative QSAR evidence for a free-radical mechanism of phenol-induced toxicity

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