Enthalpy of formation for indazoles (indazole, 1H-indazole-3-carboxylic acid, 1H-indazole-5-carboxylic acid, 1H-indazole-6-carboxylic acid and 1-methyl-1H-indazole-6-carboxylic methyl ester): experimental and theoretical studies-Reference-Cited by-同舟云学术

Enthalpy of formation for indazoles (indazole, 1H-indazole-3-carboxylic acid, 1H-indazole-5-carboxylic acid, 1H-indazole-6-carboxylic acid and 1-methyl-1H-indazole-6-carboxylic methyl ester): experimental and theoretical studies

Published:2019-11-27 Issue:2 Volume:141 Page:819-828
ISSN:1388-6150
Container-title:Journal of Thermal Analysis and Calorimetry
language:en
Short-container-title:J Therm Anal Calorim

Author:

Orozco-Guareño E.^ORCID,Campos J. Baudelio,Bárcena-Soto Maximiliano,Zúñiga-Gutierrez Bernardo

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Springer Science and Business Media LLC

Link

http://link.springer.com/content/pdf/10.1007/s10973-019-09078-8.pdf

Reference57 articles.

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3. Yamaguchi M, et al. Novel antiasthmatic agents with dual activities of thromboxane A2 synthetase inhibition and bronchodilation. VI. Indazole derivatives. Chem Pharm Bull. 1995;43(2):332–4.

4. Byung Chul K, Jin Il K, Yurngdong J. A versatile synthesis of 3-substituted indazoles. Korean Chem Soc. 1991;14(2):97–8.

5. De Lucca GV, et al. Nonsymmetric P2/P2′ cyclic urea HIV protease inhibitors. Structure–activity relationship, bioavailability, and resistance profile of monoindazole-substituted P2 analogues. J Med Chem. 1998;2623(98):2411–23.

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