Azide and Solvent Trapping of Electrophilic Intermediates Generated during the Hydrolysis of N-(Sulfonatooxy)-N-acetyl-4-aminostilbene
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, Miami University, Oxford, Ohio 45056
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo980500z
Reference22 articles.
1. N-Aryl-N-acetylnitrenium ions in aromatic amine carcinogenesis. 4
2. Reaction of trans-4-N-acetoxy-N-acetylaminostilbene with guanosine and deoxyguanosine in vitro: The primary reaction product at N2 of guanine yields different final adducts
3. Deamination of 1-methylcytosine by the carcinogen N-acetoxy-4-acetamidostilbene: implications for hydrocarbon carcinogenesis
4. Reactivity Patterns of N-Arylnitrenium Ions: Lack of Correlation with .sigma.+
5. Selective Trapping of N-Acetyl-N-(4-biphenylyl)nitrenium and N-Acetyl-N-(2-fluorenyl)nitrenium Ions by 2'-Deoxyguanosine in Aqueous Solution
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