Electrophilic Chemistry of Thia-PAHs: Stable Carbocations (NMR and DFT), S-Alkylated Onium Salts, Model Electrophilic Substitutions (Nitration and Bromination), and Mutagenicity Assay-Reference-Cited by-同舟云学术

Electrophilic Chemistry of Thia-PAHs: Stable Carbocations (NMR and DFT), S-Alkylated Onium Salts, Model Electrophilic Substitutions (Nitration and Bromination), and Mutagenicity Assay

Published:2007-10-01 Issue:22 Volume:72 Page:8383-8393
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Laali Kenneth K.¹,Chun Joong-Hyun¹,Okazaki Takao¹,Kumar Subodh²,Borosky Gabriela L.³,Swartz Carol⁴

Affiliation:

1. Department of Chemistry, Kent State University, Kent, Ohio 44242

2. Environmental Toxicology and Chemistry Laboratory, Great Lakes Center, State University of New York, College at Buffalo, Buffalo, New York 14222

3. Unidad de Matemática y Física, INFIQC, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Ciudad Universitaria, Córdoba 5000, Argentina

4. Environmental Carcinogenesis Division, US Environmental Protection Agency, Research Triangle Park, North Carolina 27711

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo701502y

Reference25 articles.

1. Synthesis and mutagenicity of trans-dihydrodiol metabolites of benzo[b]naphtho[2,1-d]thiophene

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