Electrochemically promoted decarboxylative borylation of alkyl N-hydroxyphthalimide esters
An electrochemically promoted decarboxylative borylation reaction is reported. The reaction proceeds under mild conditions in an undivided cell without use of transition metal- or photo-catalysts. The key feature of the reaction is the compatibility of diboron reagents with the electrochemical condi...
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| Veröffentlicht in: | Chinese chemical letters 2022-03, Vol.33 (3), p.1555-1558 |
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| container_issue | 3 |
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| container_title | Chinese chemical letters |
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| creator | Dai, Jian-Jun Teng, Xin-Xin Fang, Wen Xu, Jun Xu, Hua-Jian |
| description | An electrochemically promoted decarboxylative borylation reaction is reported. The reaction proceeds under mild conditions in an undivided cell without use of transition metal- or photo-catalysts. The key feature of the reaction is the compatibility of diboron reagents with the electrochemical conditions. This reaction exhibits broad substrate scope, good functional group tolerability, and easy scalability.
An electrochemically promoted decarboxylative borylation reaction is reported. The reaction proceeds under mild conditions in an undivided cell without use of transition metal- or photo-catalysts. [Display omitted] |
| doi_str_mv | 10.1016/j.cclet.2021.09.011 |
| format | Article |
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An electrochemically promoted decarboxylative borylation reaction is reported. The reaction proceeds under mild conditions in an undivided cell without use of transition metal- or photo-catalysts. [Display omitted]</description><subject>Alkyl boronic esters</subject><subject>Borylation</subject><subject>Decarboxylation</subject><subject>Electrochemical</subject><subject>Redox active esters</subject><issn>1001-8417</issn><issn>1878-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kDtPw0AQhC0EEiHwC2jcUdncw8-CAkXhIUXQQENzOu-t43POvuhsIObXc0moqXaKmVnNFwTXlMSU0Oy2jQEMjjEjjMakjAmlJ8GMFnkRpWWWnHpNCI2KhObnwcUwtISwouDZLPhYGoTRWWiw0yCNmcKts50dUYUKQbrK7iYjR_2FYWXdQdo-tHUozWYy4UvUTMp5z7YZG2l0pxWGOIzohsvgrJZmwKu_Ow_eH5Zvi6do9fr4vLhfRcB5OkYACchUFUWFLCvzMqkzVaV5BYxBXZW5hDRl4GcUss6QZzxXNGE84QlN01LWfB7cHHu_ZV_Lfi1a--l6_1H8rJvdpvJQGOEkz7yTH53g7DA4rMXW6U66SVAi9iBFKw4gxR6kIKXwIH3q7phCP-JLoxMDaOwBlXaenVBW_5v_BWKDf3s</recordid><startdate>20220301</startdate><enddate>20220301</enddate><creator>Dai, Jian-Jun</creator><creator>Teng, Xin-Xin</creator><creator>Fang, Wen</creator><creator>Xu, Jun</creator><creator>Xu, Hua-Jian</creator><general>Elsevier B.V</general><general>Anhui Province Key Laboratory of Advance Catalytic Materials and Reaction Engineering,Hefei University of Technology,Hefei 230009,China%School of Food and Biological Engineering,Hefei University of Technology,Hefei 230009,China</general><general>School of Food and Biological Engineering,Hefei University of Technology,Hefei 230009,China</general><scope>AAYXX</scope><scope>CITATION</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope><orcidid>https://orcid.org/0000-0001-7918-0080</orcidid></search><sort><creationdate>20220301</creationdate><title>Electrochemically promoted decarboxylative borylation of alkyl N-hydroxyphthalimide esters</title><author>Dai, Jian-Jun ; Teng, Xin-Xin ; Fang, Wen ; Xu, Jun ; Xu, Hua-Jian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c335t-cc4ca5d88be269794f6db57bc22cfb97ac552c5968af6e3637d14234341559af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alkyl boronic esters</topic><topic>Borylation</topic><topic>Decarboxylation</topic><topic>Electrochemical</topic><topic>Redox active esters</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dai, Jian-Jun</creatorcontrib><creatorcontrib>Teng, Xin-Xin</creatorcontrib><creatorcontrib>Fang, Wen</creatorcontrib><creatorcontrib>Xu, Jun</creatorcontrib><creatorcontrib>Xu, Hua-Jian</creatorcontrib><collection>CrossRef</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese chemical letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dai, Jian-Jun</au><au>Teng, Xin-Xin</au><au>Fang, Wen</au><au>Xu, Jun</au><au>Xu, Hua-Jian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemically promoted decarboxylative borylation of alkyl N-hydroxyphthalimide esters</atitle><jtitle>Chinese chemical letters</jtitle><date>2022-03-01</date><risdate>2022</risdate><volume>33</volume><issue>3</issue><spage>1555</spage><epage>1558</epage><pages>1555-1558</pages><issn>1001-8417</issn><eissn>1878-5964</eissn><abstract>An electrochemically promoted decarboxylative borylation reaction is reported. The reaction proceeds under mild conditions in an undivided cell without use of transition metal- or photo-catalysts. The key feature of the reaction is the compatibility of diboron reagents with the electrochemical conditions. This reaction exhibits broad substrate scope, good functional group tolerability, and easy scalability.
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| fulltext | fulltext |
| identifier | ISSN: 1001-8417 |
| ispartof | Chinese chemical letters, 2022-03, Vol.33 (3), p.1555-1558 |
| issn | 1001-8417 1878-5964 |
| language | eng |
| recordid | cdi_wanfang_journals_zghxkb202203076 |
| source | Elsevier ScienceDirect Journals Complete; Alma/SFX Local Collection |
| subjects | Alkyl boronic esters Borylation Decarboxylation Electrochemical Redox active esters |
| title | Electrochemically promoted decarboxylative borylation of alkyl N-hydroxyphthalimide esters |
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