{"id":12223,"date":"2023-02-09T10:51:05","date_gmt":"2023-02-09T02:51:05","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=12223"},"modified":"2023-02-09T10:51:05","modified_gmt":"2023-02-09T02:51:05","slug":"cativiela-c-et-al-published-their-research-in-anales-de-quimica-serie-c-quimica-organica-y-bioquimica-in-1987-cas-10199-53-8","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=12223","title":{"rendered":"Cativiela, C. et al. published their research in Anales de Quimica, Serie C:  Quimica Organica y Bioquimica in 1987 | CAS: 10199-53-8"},"content":{"rendered":"<p>Application of Free-Wilson models in spectroscopy. Reevaluation of the Tensmeyer additivity system in the proton NMR of pyrazoles was written by Cativiela, C.;Garcia, J. I.;Elguero, J.. And the article was included in Anales de Quimica, Serie C:  Quimica Organica y Bioquimica in 1987.<a href=\"https:\/\/www.ambeed.com\/products\/10199-53-8.html\">Electric Literature of C11H10N2O2<\/a> This article mentions the following:<\/p>\n<p>Modified coefficients of the Tensmeyer additivity system are used to calculate <sup>1<\/sup>H NMR chem. shifts \u03b4(4-H) of the proton at the 4-position of 1,3,5-substituted pyrazoles. The coefficients were reevaluated by using a more accurate math. procedure. In the experiment, the researchers used many compounds, for example, 1-Methyl-5-phenyl-1H-pyrazole-3-carboxylic acid (cas: 10199-53-8<a href=\"https:\/\/www.ambeed.com\/products\/10199-53-8.html\">Electric Literature of C11H10N2O2<\/a>).<\/p>\n<p>1-Methyl-5-phenyl-1H-pyrazole-3-carboxylic acid (cas: 10199-53-8) belongs to pyrazole derivatives. An alternative way to synthesize multisubstituted pyrazoles is the Csingle bondH arylation of simple pyrazoles. Pyrazole rings have been used as core components of several leading non-steroidal anti-inflammatory drugs (NSAIDs) and antihypertensive drugs. It has also been found to be useful as a bifunctional ligand for metal catalysis.<a href=\"https:\/\/www.ambeed.com\/products\/10199-53-8.html\">Electric Literature of C11H10N2O2<\/a><\/p>\n<p>Referemce:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">Pyrazole &#8211; Wikipedia<\/a>,<br \/><a href=\"https:\/\/www.sciencedirect.com\/topics\/chemistry\/pyrazoles\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>1-Methyl-5-phenyl-1H-pyrazole-3-carboxylic acid (cas: 10199-53-8) belongs to pyrazole derivatives. An alternative way to synthesize multisubstituted pyrazoles is the Csingle bondH arylation of simple pyrazoles. Pyrazole rings have been used as core components of several leading non-steroidal anti-inflammatory drugs (NSAIDs) and antihypertensive drugs. It has also been found to be useful as a bifunctional ligand for metal catalysis.<a href=\"https:\/\/www.ambeed.com\/products\/10199-53-8.html\">Electric Literature of C11H10N2O2<\/a><\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[836,131],"tags":[129],"class_list":["post-12223","post","type-post","status-publish","format-standard","hentry","category-10199-53-8","category-pyrazoles-derivatives","tag-200-300"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Cativiela, C. et al. published their research in Anales de Quimica, Serie C: Quimica Organica y Bioquimica in 1987 | CAS: 10199-53-8 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Application of Free-Wilson models in spectroscopy. Reevaluation of the Tensmeyer additivity system in the proton NMR of pyrazoles was written by Cativiela, C.;Garcia, J. I.;Elguero, J.. And the article was included in Anales de Quimica, Serie C: Quimica Organica y Bioquimica in 1987.Electric Literature of C11H10N2O2 This article mentions the following:\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.pyrazoles-derivatives.com\/?p=12223\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Cativiela, C. et al. published their research in Anales de Quimica, Serie C: Quimica Organica y Bioquimica in 1987 | CAS: 10199-53-8 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"Application of Free-Wilson models in spectroscopy. Reevaluation of the Tensmeyer additivity system in the proton NMR of pyrazoles was written by Cativiela, C.;Garcia, J. I.;Elguero, J.. 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Reevaluation of the Tensmeyer additivity system in the proton NMR of pyrazoles was written by Cativiela, C.;Garcia, J. I.;Elguero, J.. 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Reevaluation of the Tensmeyer additivity system in the proton NMR of pyrazoles was written by Cativiela, C.;Garcia, J. I.;Elguero, J.. And the article was included in Anales de Quimica, Serie C: Quimica Organica y Bioquimica in 1987.Electric Literature of C11H10N2O2 This article mentions the following:","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.pyrazoles-derivatives.com\/?p=12223","og_locale":"en_US","og_type":"article","og_title":"Cativiela, C. et al. published their research in Anales de Quimica, Serie C: Quimica Organica y Bioquimica in 1987 | CAS: 10199-53-8 | pyrazoles-derivatives","og_description":"Application of Free-Wilson models in spectroscopy. Reevaluation of the Tensmeyer additivity system in the proton NMR of pyrazoles was written by Cativiela, C.;Garcia, J. I.;Elguero, J.. 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