Michael Novak

Affiliations: 
Miami University (Ohio), Oxford, OH 
Area:
Organic Chemistry
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"Michael Novak"
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Zhang Y, Chakraborty M, Cerda-Smith CG, et al. (2013) Chemistry of ring-substituted 4-(benzothiazol-2-yl)phenylnitrenium ions from antitumor 2-(4-aminophenyl)benzothiazoles. The Journal of Organic Chemistry. 78: 6992-7000
Chakraborty M, Brzozowski CF, Novak M. (2012) Reversible formation of aryloxenium ions from the corresponding quinols under acidic conditions Journal of Physical Organic Chemistry. 25: 1236-1242
Rumpel A, Novak M, Walter J, et al. (2011) Tuning the molecular order of C60 functionalized phosphonic acid monolayers. Langmuir : the Acs Journal of Surfaces and Colloids. 27: 15016-23
Novak M, Chakraborty M. (2011) Reactions of a putative metabolite of the model antitumor drug 2-(4-aminophenyl)benzothiazole with purines and pyrimidines Journal of Physical Organic Chemistry. 24: 960-968
Chakraborty M, Jin KJ, Glover SA, et al. (2010) Characterization of the 4-(benzothiazol-2-yl)phenylnitrenium ion from a putative metabolite of a model antitumor drug. The Journal of Organic Chemistry. 75: 5296-304
Novak M, Chakraborty M. (2010) N‐Arylhydroxylamines and Chemical Carcinogenicity Patai's Chemistry of Functional Groups
Chakraborty M, Jin KJ, Brewer SC, et al. (2009) Indirect and direct detection of the 4-(benzothiazol-2-yl)phenylnitrenium ion from a putative metabolite of a model anti-tumor drug. Organic Letters. 11: 4862-5
Wang YT, Novak M. (2009) Multiple decomposition pathways for the oxenium ion precursor O-(4-(4'-methylphenyl)phenyl)-N-methanesulfonylhydroxylamine. The Journal of Organic Chemistry. 74: 7697-706
Wang YT, Jin KJ, Myers LR, et al. (2009) Hydrolysis and photolysis of 4-Acetoxy-4-(benzothiazol-2-yl)-2,5-cyclohexadien-1-one, a model anti-tumor quinol ester. The Journal of Organic Chemistry. 74: 4463-71
Wang YT, Jin KJ, Leopold SH, et al. (2008) Characterization of reactive intermediates generated during photolysis of 4-acetoxy-4-aryl-2,5-cyclohexadienones: oxenium ions and aryloxy radicals. Journal of the American Chemical Society. 130: 16021-30
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