Theoretical Calculation of Substituent Effects on the O−H Bond Strength of Phenolic Antioxidants Related to Vitamin E-Reference-Cited by-同舟云学术

Theoretical Calculation of Substituent Effects on the O−H Bond Strength of Phenolic Antioxidants Related to Vitamin E

Published:1997-05-01 Issue:18 Volume:119 Page:4245-4252
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wright James S.¹,Carpenter David J.¹,McKay Daniel J.¹,Ingold K. U.¹

Affiliation:

1. Contribution from the Department of Chemistry, Ottawa−Carleton Chemistry Institute, Carleton University, 1125 Colonel By Drive, Ottawa, Canada K1S 5B, and Steacie Institute for Molecular Sciences, National Research Council of Canada, Ottawa, Canada K1A 0R6

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja963378z

Reference42 articles.

1. Burton, G. W.; Joyce, A.; Ingold, K. U.Lancet1982,August, 751. Burton, G. W.; Joyce, A.; Ingold, K. U.Arch. Biochem. Biophys.1983,221, 281−289. Ingold, K. U.; Webb, A. C.; Witter, D.; Burton, G. W.; Metcalf, T. A.; Muller, D. P. R.Arch. Biochem. Biophys.1987,259, 224−225.

2. Lipid Peroxidation and Lipid Antioxidants in Normal and Tumor Cells

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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