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Alan R. Katritzky
Researcher at University of Florida
Publications - 1988
Citations - 35516
Alan R. Katritzky is an academic researcher from University of Florida. The author has contributed to research in topics: Benzotriazole & Alkyl. The author has an hindex of 73, co-authored 1988 publications receiving 33831 citations. Previous affiliations of Alan R. Katritzky include University of North Texas & University of Akron.
Papers
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Journal ArticleDOI
Mechanism-Based QSAR Modeling of Skin Sensitization.
John C. Dearden,Mark Hewitt,David W. Roberts,Steven J. Enoch,P H Rowe,Katarzyna R. Przybylak,G. D. Vaughan-Williams,M. L. Smith,Girinath G. Pillai,Girinath G. Pillai,Alan R. Katritzky +10 more
TL;DR: Using two large published data sets of skin sensitizers, each sensitizing chemical is allocated to one of 10 mechanistic categories and good QSAR models for the seven categories that have a sufficient number of chemicals to allow modeling.
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The conformational analysis of saturated heterocycles. Part XLV. N-Alkyldihydro-1,3,5-dithiazines and N-alkyltetrahydro-1,3,5-thiadiazines
TL;DR: In this paper, the synthesis, low-temperature n.m.r. spectra, and coalescence ΔG* for ring inversion, and dipole moments of the title compounds are discussed, together with the predominant conformations of these compounds.
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QSAR modeling of blood:air and tissue:air partition coefficients using theoretical descriptors
Alan R. Katritzky,Minati Kuanar,Dan C. Fara,Mati Karelson,William E. Acree,Vitaly P. Solov'ev,Alexandre Varnek +6 more
TL;DR: Human blood:air, human and rat tissue:air partition coefficients of a diverse set of organic compounds were correlated and predicted using structural descriptors by employing CODESSA-PRO and ISIDA programs.
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Peptidomimetics via Modifications of Amino Acids and Peptide Bonds
TL;DR: A review of peptidomimetics that are formed via heteroatom replacement within the native amino acid backbone can be found in this article, where structural features, utility and preparative methods are discussed.
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Conjugated systems derived from piperazine‐2,5‐dione
TL;DR: In this article, the preparation of mono-and unsymmetrical bis-ylidine derivatives of piperazine-2,5-dione is described and the uv-visible absorption of the products is correlated with acceptor/donor character of the substituents.