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Chemical Research in Toxicology|April 1, 1995
o-Methoxy-4-alkylphenols that form quinone methides of intermediate reactivity are the most toxic in rat liver slicesD C Thompson, K Perera, E S Krol, et al.
Archives of Environmental Contamination and Toxicology|January 31, 1998
Comparative bioaccumulation of chlorinated hydrocarbons from sediment by two infaunal invertebratesJ P Meador, N G Adams, E Casillas, et al.
Chemical Research in Toxicology|January 1, 1990
Formation and reactivity of alternative quinone methides from butylated hydroxytoluene: possible explanation for species-specific pneumotoxicityJ L Bolton, H Sevestre, B O Ibe, et al.
Chemical Research in Toxicology|June 1, 1995
The influence of the p-alkyl substituent on the isomerization of o-quinones to p-quinone methides: potential bioactivation mechanism for catecholsS L Iverson, L Q Hu, V Vukomanovic, et al.
Chemical Research in Toxicology|December 1, 1996
Alkylation of 2'-deoxynucleosides and DNA by quinone methides derived from 2,6-di-tert-butyl-4-methylphenolM A Lewis, D G Yoerg, J L Bolton, et al.
Memory & Cognition|January 1, 1989
Speakers' assumptions about the lexical flexibility of idiomsR W Gibbs, N P Nayak, J L Bolton, et al.
Combinatorial Chemistry & High Throughput Screening|July 27, 1999
Screening for xenobiotic electrophilic metabolites using pulsed ultrafiltration-mass spectrometryD Nikolic, P W Fan, J L Bolton, et al.
Chemico-Biological Interactions|April 14, 1995
Reaction of glutathione with the electrophilic metabolites of 1,1-dichloroethyleneT F Dowsley, P G Forkert, L A Benesch, et al.
Chemical Research in Toxicology|June 21, 2001
Synthesis and reactivity of the catechol metabolites from the equine estrogen, 8,9-dehydroestroneF Zhang, D Yao, Y Hua, et al.
Chemical Research in Toxicology|August 1, 1997
Oxo substituents markedly alter the phase II metabolism of alpha-hydroxybutenylbenzenes: models probing the bioactivation mechanisms of tamoxifenK V Ramakrishna, P W Fan, C S Boyer, et al.
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