Substituent Effects and Charge Delocalization Mode in Chrysenium, Benzo[c]phenanthrenium, and Benzo[g]chrysenium Cations: A Stable Ion and Electrophilic Substitution Study-Reference-Cited by-同舟云学术

Substituent Effects and Charge Delocalization Mode in Chrysenium, Benzo[c]phenanthrenium, and Benzo[g]chrysenium Cations: A Stable Ion and Electrophilic Substitution Study

Published:2001-01-16 Issue:3 Volume:66 Page:780-788
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Laali Kenneth K.¹,Okazaki Takao¹,Kumar Subodh²,Galembeck Sergio E.³

Affiliation:

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

2. Environmental Toxicology & Chemistry, Great Lakes Center for Environmental Research and Education, State University of New York College at Buffalo, 1300 Elmwood Avenue, Buffalo, New York 14222

3. LAMMOL, Departamento de Quimica, FFCLRP-USP, SP-Brazil

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo001268b

Reference40 articles.

1. Coombs, M. M.; Bhatt, T. S.Cyclopenta[a]phenanthrene; Cambridge University Press: Cambridge, UK, 1987; Chapter 6.

2. Synthesis of anti- and syn-Diol Epoxides of trans-3,4-Dihydroxy-3,4-dihydrobenzo[ghi]fluoranthene: Model Planar Diol Epoxides

3. Efficient Syntheses of the anti- and syn-Diol Epoxide Metabolites of the Carcinogenic Polycyclic Aromatic Hydrocarbon Benzo[g]chrysene

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