{"id":10133,"date":"2022-10-17T02:49:11","date_gmt":"2022-10-16T18:49:11","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=10133"},"modified":"2022-10-17T02:49:11","modified_gmt":"2022-10-16T18:49:11","slug":"song-baos-team-published-research-in-molecular-catalysis-in-2021-11-30-13788-92-6","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=10133","title":{"rendered":"Song, Bao&#8217;s team published research in Molecular Catalysis  in 2021-11-30 | 13788-92-6"},"content":{"rendered":"<p>Song, Bao; Cao, Ningtao; Zhang, Jie; Xie, Jianwei published the artcile< Copper pyrithione (CuPT)-catalyzed\/mediated amination and thioarylation of (hetero)aryl halides: A competition>,  <a href=\"https:\/\/www.ambeed.com\/products\/13788-92-6.html\">Electric Literature of 13788-92-6<\/a>,  the main research area is  arylhalide pyrazole copper pyrithione catalyst amination coupling reaction; arylpyrazole preparation; copper pyrithione aryl halide thioarylation coupling reaction; aryl thiopyridineoxide preparation.<\/p>\n<p>A facile method for the synthesis of N-arylheterocycles and di(hetero)aryl sulfides under mild condition was described. In these transformations, copper pyrithione (CuPT) was used as the copper catalyst for CN coupling, while served as catalyst and coupled partner for CS coupling with high yields and broad substrate tolerance. The S-arylation process was also utilized for the construction of valuable bioactive 2-sulfonylpyridine 1-oxide derivatives<\/p>\n<p>Molecular Catalysis published new progress about Amination. 13788-92-6 belongs to class pyrazoles-derivatives, and the molecular formula is C9H7BrN2, <a href=\"https:\/\/www.ambeed.com\/products\/13788-92-6.html\">Electric Literature of 13788-92-6<\/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>Molecular Catalysis published new progress about Amination. 13788-92-6 belongs to class pyrazoles-derivatives, and the molecular formula is C9H7BrN2, <a href=\"https:\/\/www.ambeed.com\/products\/13788-92-6.html\">Electric Literature of 13788-92-6<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[738,131],"tags":[716],"class_list":["post-10133","post","type-post","status-publish","format-standard","hentry","category-13788-92-6","category-pyrazoles-derivatives","tag-m-w200-250"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Song, Bao&#039;s team published research in Molecular Catalysis in 2021-11-30 | 13788-92-6 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Song, Bao; Cao, Ningtao; Zhang, Jie; Xie, Jianwei published the artcile&lt; Copper pyrithione (CuPT)-catalyzed\/mediated amination and thioarylation of (hetero)aryl halides: A competition&gt;, Electric Literature of 13788-92-6, the main research area is arylhalide pyrazole copper pyrithione catalyst amination coupling reaction; arylpyrazole preparation; copper pyrithione aryl halide thioarylation coupling reaction; aryl thiopyridineoxide preparation.\" \/>\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=10133\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Song, Bao&#039;s team published research in Molecular Catalysis in 2021-11-30 | 13788-92-6 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"Song, Bao; Cao, Ningtao; Zhang, Jie; Xie, Jianwei published the artcile&lt; Copper pyrithione (CuPT)-catalyzed\/mediated amination and thioarylation of (hetero)aryl halides: A competition&gt;, Electric Literature of 13788-92-6, the main research area is arylhalide pyrazole copper pyrithione catalyst amination coupling reaction; arylpyrazole preparation; copper pyrithione aryl halide thioarylation coupling reaction; aryl thiopyridineoxide preparation.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.pyrazoles-derivatives.com\/?p=10133\" \/>\n<meta property=\"og:site_name\" content=\"pyrazoles-derivatives\" \/>\n<meta property=\"article:published_time\" content=\"2022-10-16T18:49:11+00:00\" \/>\n<meta name=\"author\" content=\"Jessica.F\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Jessica.F\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=10133\",\"url\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=10133\",\"name\":\"Song, Bao's team published research in Molecular Catalysis in 2021-11-30 | 13788-92-6 | pyrazoles-derivatives\",\"isPartOf\":{\"@id\":\"http:\/\/www.pyrazoles-derivatives.com\/#website\"},\"datePublished\":\"2022-10-16T18:49:11+00:00\",\"author\":{\"@id\":\"http:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\"},\"description\":\"Song, Bao; Cao, Ningtao; Zhang, Jie; Xie, Jianwei published the artcile< Copper pyrithione (CuPT)-catalyzed\/mediated amination and thioarylation of (hetero)aryl halides: A competition>, Electric Literature of 13788-92-6, the main research area is arylhalide pyrazole copper pyrithione catalyst amination coupling reaction; arylpyrazole preparation; copper pyrithione aryl halide thioarylation coupling reaction; aryl thiopyridineoxide preparation.\",\"breadcrumb\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=10133#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.pyrazoles-derivatives.com\/?p=10133\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=10133#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"\u9996\u9875\",\"item\":\"http:\/\/www.pyrazoles-derivatives.com\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Song, Bao&#8217;s team published research in Molecular Catalysis in 2021-11-30 | 13788-92-6\"}]},{\"@type\":\"WebSite\",\"@id\":\"http:\/\/www.pyrazoles-derivatives.com\/#website\",\"url\":\"http:\/\/www.pyrazoles-derivatives.com\/\",\"name\":\"pyrazoles-derivatives\",\"description\":\"Several pyrazole derivatives possess important pharmacological activities and they have been proved useful materials in drug research. Pyrazole derivatives play an important role in antitumor agents.\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"http:\/\/www.pyrazoles-derivatives.com\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Person\",\"@id\":\"http:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\",\"name\":\"Jessica.F\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"http:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/weavatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g\",\"contentUrl\":\"https:\/\/weavatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g\",\"caption\":\"Jessica.F\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Song, Bao's team published research in Molecular Catalysis in 2021-11-30 | 13788-92-6 | pyrazoles-derivatives","description":"Song, Bao; Cao, Ningtao; Zhang, Jie; Xie, Jianwei published the artcile< Copper pyrithione (CuPT)-catalyzed\/mediated amination and thioarylation of (hetero)aryl halides: A competition>, Electric Literature of 13788-92-6, the main research area is arylhalide pyrazole copper pyrithione catalyst amination coupling reaction; arylpyrazole preparation; copper pyrithione aryl halide thioarylation coupling reaction; aryl thiopyridineoxide preparation.","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=10133","og_locale":"en_US","og_type":"article","og_title":"Song, Bao's team published research in Molecular Catalysis in 2021-11-30 | 13788-92-6 | pyrazoles-derivatives","og_description":"Song, Bao; Cao, Ningtao; Zhang, Jie; Xie, Jianwei published the artcile< Copper pyrithione (CuPT)-catalyzed\/mediated amination and thioarylation of (hetero)aryl halides: A competition>, Electric Literature of 13788-92-6, the main research area is arylhalide pyrazole copper pyrithione catalyst amination coupling reaction; arylpyrazole preparation; copper pyrithione aryl halide thioarylation coupling reaction; aryl thiopyridineoxide preparation.","og_url":"https:\/\/www.pyrazoles-derivatives.com\/?p=10133","og_site_name":"pyrazoles-derivatives","article_published_time":"2022-10-16T18:49:11+00:00","author":"Jessica.F","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Jessica.F","Est. reading time":"1 minute"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=10133","url":"https:\/\/www.pyrazoles-derivatives.com\/?p=10133","name":"Song, Bao's team published research in Molecular Catalysis in 2021-11-30 | 13788-92-6 | pyrazoles-derivatives","isPartOf":{"@id":"http:\/\/www.pyrazoles-derivatives.com\/#website"},"datePublished":"2022-10-16T18:49:11+00:00","author":{"@id":"http:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1"},"description":"Song, Bao; Cao, Ningtao; Zhang, Jie; Xie, Jianwei published the artcile< Copper pyrithione (CuPT)-catalyzed\/mediated amination and thioarylation of (hetero)aryl halides: A competition>, Electric Literature of 13788-92-6, the main research area is arylhalide pyrazole copper pyrithione catalyst amination coupling reaction; arylpyrazole preparation; copper pyrithione aryl halide thioarylation coupling reaction; aryl thiopyridineoxide preparation.","breadcrumb":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=10133#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.pyrazoles-derivatives.com\/?p=10133"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=10133#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"\u9996\u9875","item":"http:\/\/www.pyrazoles-derivatives.com\/"},{"@type":"ListItem","position":2,"name":"Song, Bao&#8217;s team published research in Molecular Catalysis in 2021-11-30 | 13788-92-6"}]},{"@type":"WebSite","@id":"http:\/\/www.pyrazoles-derivatives.com\/#website","url":"http:\/\/www.pyrazoles-derivatives.com\/","name":"pyrazoles-derivatives","description":"Several pyrazole derivatives possess important pharmacological activities and they have been proved useful materials in drug research. 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