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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.

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Reactions of pyryliums with mono- and asym-di-substituted hydrazines

TL;DR: This article reviewed literature data on the title reactions and further examples given particularly with dialkylhydrazines and hydrazones, and new examples of dihydropyrazoloquinoline (27) and oxidopyrido[1,2-b]pyridazinium [(62)−(64)] ring systems are described.
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Regioselective synthesis and theoretical studies of an anti-neoplastic fluoro-substituted dispiro-oxindole

TL;DR: In this article, single crystal X-ray studies of regioselectively synthesized fluoro-substituted dispiro-oxindole 9 revealed that the structure belongs to the monoclinic space group P21/n with four molecules in the unit cell.
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Efficient Syntheses of Substituted Carbazoles and Cyclopent[b]indoles from 1-Methyl-3-(benzotriazol-1-ylmethyl)indole.

TL;DR: NMR study is described to discriminate between structures of types 6 and 8 on the basis of (1)H-(13)C long-range correlation to give 1-functionalized cyclopent[b]indoles 15 and 16 with a high degree of stereoselectivity.
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QSPR study of critical micelle concentration of anionic surfactants using computational molecular descriptors.

TL;DR: A data set of 181 diverse anionic surfactants has been investigated to relate the logarithm of critical micelle concentration to the molecular structure using Comprehensive Descriptors for Structural and Statistical Analysis (CODESSA Pro) software, and a fragment approach provided superior quantitative structure-property relationship (QSPR) models in terms of statistical characteristics and predictive ability.
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Convenient syntheses of dihydropyrrolo[2′,1′:3,4]pyrazino- and dihydropyrrolo[2′,1′:3,4][1,4]diazepino-[2,1-a]isoindolones

TL;DR: Dihydropyrrolo[2′,1′:3,4]pyrazino[2,1-a]isoindolones as discussed by the authors were obtained in 76-81% yields by the reaction of 2-(1H-pyrrol-1-yl)ethylamine with 2-formylbenzoic acids.