{"id":10005,"date":"2022-10-13T03:03:51","date_gmt":"2022-10-12T19:03:51","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=10005"},"modified":"2022-10-13T03:03:51","modified_gmt":"2022-10-12T19:03:51","slug":"obrien-alexander-g-s-team-published-research-in-angewandte-chemie-international-edition-in-2014-cas-5952-93-2","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=10005","title":{"rendered":"O&#8217;Brien, Alexander G.&#8217;s team published research in Angewandte Chemie, International Edition in 2014 | CAS: 5952-93-2"},"content":{"rendered":"<p>In 2014,Angewandte Chemie, International Edition included an article by O&#8217;Brien, Alexander G.; Maruyama, Akinobu; Inokuma, Yasuhide; Fujita, Makoto; Baran, Phil S.; Blackmond, Donna G.. <a href=\"https:\/\/www.ambeed.com\/products\/5952-93-2.html\">Category: pyrazoles-derivatives<\/a>. The article was titled \u300aRadical C-H functionalization of heteroarenes under electrochemical control\u300b. The information in the text is summarized as follows:<\/p>\n<p>Electrochem. reactions are shown to be effective for the C-H functionalization of a number of heterocyclic substrates that are recalcitrant to conventional peroxide radical initiation conditions. Monitoring reaction progress under electrochem. conditions provides mechanistic insight into the C-H functionalization of a series of heterocycles of interest in medicinal chem. In addition to this study using Methyl 1-methyl-1H-pyrazole-4-carboxylate, there are many other studies that have used Methyl 1-methyl-1H-pyrazole-4-carboxylate(cas: 5952-93-2<a href=\"https:\/\/www.ambeed.com\/products\/5952-93-2.html\">Category: pyrazoles-derivatives<\/a>) was used in this study.<\/p>\n<p>Methyl 1-methyl-1H-pyrazole-4-carboxylate(cas: 5952-93-2) belongs to pyrazoles. Pyrazoles and their related multiring analogs are common elements of a wide variety of bioactive compounds. These ring structures are rare in nature. A consequence of this is that they have previously been thought to be poor moieties to include in potential new drugs. <a href=\"https:\/\/www.ambeed.com\/products\/5952-93-2.html\">Category: pyrazoles-derivatives<\/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>Methyl 1-methyl-1H-pyrazole-4-carboxylate(cas: 5952-93-2) belongs to pyrazoles. Pyrazoles and their related multiring analogs are common elements of a wide variety of bioactive compounds. These ring structures are rare in nature. A consequence of this is that they have previously been thought to be poor moieties to include in potential new drugs. <a href=\"https:\/\/www.ambeed.com\/products\/5952-93-2.html\">Category: pyrazoles-derivatives<\/a><\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[689,131],"tags":[128],"class_list":["post-10005","post","type-post","status-publish","format-standard","hentry","category-5952-93-2","category-pyrazoles-derivatives","tag-100-200"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>O&#039;Brien, Alexander G.&#039;s team published research in Angewandte Chemie, International Edition in 2014 | CAS: 5952-93-2 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"In 2014,Angewandte Chemie, International Edition included an article by O&#039;Brien, Alexander G.; Maruyama, Akinobu; Inokuma, Yasuhide; Fujita, Makoto; Baran, Phil S.; Blackmond, Donna G.. Category: pyrazoles-derivatives. The article was titled \u300aRadical C-H functionalization of heteroarenes under electrochemical control\u300b. The information in the text is summarized as follows:\" \/>\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=10005\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"O&#039;Brien, Alexander G.&#039;s team published research in Angewandte Chemie, International Edition in 2014 | CAS: 5952-93-2 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"In 2014,Angewandte Chemie, International Edition included an article by O&#039;Brien, Alexander G.; Maruyama, Akinobu; Inokuma, Yasuhide; Fujita, Makoto; Baran, Phil S.; Blackmond, Donna G.. Category: pyrazoles-derivatives. The article was titled \u300aRadical C-H functionalization of heteroarenes under electrochemical control\u300b. 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