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Ground states of conjugated molecules. XIX. Tautomerism of heteroaromatic hydroxy and amino derivatives and nucleotide bases

Nicolae Bodor, +2 more
- 01 May 1970 - 
- Vol. 92, Iss: 10, pp 2929-2936
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This article is published in Journal of the American Chemical Society.The article was published on 1970-05-01. It has received 125 citations till now. The article focuses on the topics: Tautomer.

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Synthesis of Tri- and Tetrasubstituted Furans Catalyzed by Trifluoroacetic Acid

TL;DR: Substituted 2-hydroxy-3-acetylfurans are synthesized by alkylation of tert-butyl acetoacetate with an alpha-haloketone followed by treatment of the obtained intermediate with trifluoroacetic acid (TFA).
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AN EPR STUDY OF π‐CATION RADICALS IN DINUCLEOSIDE PHOSPHATES AND DNA PRODUCED BY PHOTOIONIZATION

TL;DR: In this article, the guanine cation was found to be formed preferentially by photolysis of mixed dinucleoside phosphates, e.g., TpT, GpG, or dApdA.
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Tautomerie und Nomenklatur der „Pyrazolone”︁ und Amino‐pyrazole

TL;DR: In this paper, a logiscale nomenklaturaheliche and logische Nomenklature empfohlen for the pyrazolone is presented, wobei alle N-substituierten „Pyrazolones” sollten in Zukunft nach der tautomeren Form benannt werden.
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Quinoline-based HIV Integrase Inhibitors

TL;DR: This review is focused on those compounds that have a quinoline scaffold and attempts to answer the question of whether quin Caroline is privileged for these activities of HIV integrase.
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A non-empirical molecular orbital study on the relative stabilities of adenine and guanine tautomers

TL;DR: The relative stabilities of a series of adenine and guanine tautomers have been calculated using anab initio Hartree-Fock-Roothaan SCF MO method as mentioned in this paper.
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