Electrophilic chemistry of thia-PAHs: Stable carbocations (NMR and DFT), S-alkylated onium salts, model electrophilic substitutions (nitration and bromination), and mutagenicity assay

Kenneth K. Laali; Joong Hyun Chun; Takao Okazaki; Subodh Kumar; Gabriela L. Borosky; Carol Swartz

doi:10.1021/jo701502y

Electrophilic chemistry of thia-PAHs: Stable carbocations (NMR and DFT), S-alkylated onium salts, model electrophilic substitutions (nitration and bromination), and mutagenicity assay

Kenneth K. Laali
, Joong Hyun Chun
, Takao Okazaki
, Subodh Kumar
, Gabriela L. Borosky
, Carol Swartz

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	8383-8393
Number of pages	11
Journal	Journal of Organic Chemistry
Volume	72
Issue number	22
DOIs	https://doi.org/10.1021/jo701502y
State	Published - Oct 26 2007
Externally published	Yes

ASJC Scopus Subject Areas

Organic Chemistry

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10.1021/jo701502y

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Electrophilic chemistry of thia-PAHs: Stable carbocations (NMR and DFT), S-alkylated onium salts, model electrophilic substitutions (nitration and bromination), and mutagenicity assay. / Laali, Kenneth K.; Chun, Joong Hyun; Okazaki, Takao et al.
In: Journal of Organic Chemistry, Vol. 72, No. 22, 26.10.2007, p. 8383-8393.

Research output: Contribution to journal › Article › peer-review

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AU - Kumar, Subodh

AU - Borosky, Gabriela L.

AU - Swartz, Carol

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Electrophilic chemistry of thia-PAHs: Stable carbocations (NMR and DFT), S-alkylated onium salts, model electrophilic substitutions (nitration and bromination), and mutagenicity assay

ASJC Scopus Subject Areas

Access to Document

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