Photocatalytic redox-neutral α-C(sp 3 )-H pyridination of glycine derivatives and N -arylamines with cyanopyridines
A photo-induced α-C(sp )-H decyanative pyridination of -arylglycine derivatives with cyanopyridines was developed. This reaction was performed under organic photocatalytic and redox-neutral conditions a radical-radical cross-coupling process. Besides, the protocol was also suitable for the C(sp )-H...
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| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2024-04, Vol.60 (33), p.4451-4454 |
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| container_issue | 33 |
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| container_title | Chemical communications (Cambridge, England) |
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| creator | Pan, Changduo Chen, Dongdong Cheng, Yangjian Yu, Jin-Tao |
| description | A photo-induced α-C(sp
)-H decyanative pyridination of
-arylglycine derivatives with cyanopyridines was developed. This reaction was performed under organic photocatalytic and redox-neutral conditions
a radical-radical cross-coupling process. Besides, the protocol was also suitable for the C(sp
)-H pyridination of
-aryl tetrahydroisoquinolines as well as benzylamines. |
| doi_str_mv | 10.1039/d4cc00906a |
| format | Article |
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)-H decyanative pyridination of
-arylglycine derivatives with cyanopyridines was developed. This reaction was performed under organic photocatalytic and redox-neutral conditions
a radical-radical cross-coupling process. Besides, the protocol was also suitable for the C(sp
)-H pyridination of
-aryl tetrahydroisoquinolines as well as benzylamines.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/d4cc00906a</identifier><identifier>PMID: 38563645</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Amines ; Cross coupling ; Glycine ; Organic compounds</subject><ispartof>Chemical communications (Cambridge, England), 2024-04, Vol.60 (33), p.4451-4454</ispartof><rights>Copyright Royal Society of Chemistry 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315t-914e54b1d325562f685b9b9614a29ad7f59bd5e694de1634bd5745561f8443733</citedby><cites>FETCH-LOGICAL-c315t-914e54b1d325562f685b9b9614a29ad7f59bd5e694de1634bd5745561f8443733</cites><orcidid>0000-0002-0264-9407 ; 0000-0001-5878-3835</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38563645$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pan, Changduo</creatorcontrib><creatorcontrib>Chen, Dongdong</creatorcontrib><creatorcontrib>Cheng, Yangjian</creatorcontrib><creatorcontrib>Yu, Jin-Tao</creatorcontrib><title>Photocatalytic redox-neutral α-C(sp 3 )-H pyridination of glycine derivatives and N -arylamines with cyanopyridines</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>A photo-induced α-C(sp
)-H decyanative pyridination of
-arylglycine derivatives with cyanopyridines was developed. This reaction was performed under organic photocatalytic and redox-neutral conditions
a radical-radical cross-coupling process. Besides, the protocol was also suitable for the C(sp
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-aryl tetrahydroisoquinolines as well as benzylamines.</description><subject>Amines</subject><subject>Cross coupling</subject><subject>Glycine</subject><subject>Organic compounds</subject><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpd0ctOxCAUAFBiNL43foAhcaMmKAyPKUtTn4lRF5q4ayhQxXTKCHS0n-WP-E0yOrqQDa9zb-BeAHYIPiKYymPDtMZYYqGWwDqhgiHOisfl-ZpLNKaMr4GNGF9wHoQXq2CNFlxkx9dBunv2yWuVVDskp2Gwxr-jzvYpqBZ-fqByP04hhQfoEk6H4IzrVHK-g76BT-2gXWehscHN8unMRqg6A28gUmFo1SRfRvjm0jPUg-r8It7GLbDSqDba7cW8CR7Oz-7LS3R9e3FVnlwjTQlPSBJmOauJoSPOxagRBa9lLQVhaiSVGTdc1oZbIZmxRFCWN2OWJWkKxuiY0k2w_5N3Gvxrb2OqJi5q27aqs76PFcWU5BrhEc907x998X3o8uuyYpjiAlOR1eGP0sHHGGxTTYOb5M9WBFfzXlSnrCy_e3GS8e4iZV9PrPmjv8WnX4NVg94</recordid><startdate>20240418</startdate><enddate>20240418</enddate><creator>Pan, Changduo</creator><creator>Chen, Dongdong</creator><creator>Cheng, Yangjian</creator><creator>Yu, Jin-Tao</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0264-9407</orcidid><orcidid>https://orcid.org/0000-0001-5878-3835</orcidid></search><sort><creationdate>20240418</creationdate><title>Photocatalytic redox-neutral α-C(sp 3 )-H pyridination of glycine derivatives and N -arylamines with cyanopyridines</title><author>Pan, Changduo ; Chen, Dongdong ; Cheng, Yangjian ; Yu, Jin-Tao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-914e54b1d325562f685b9b9614a29ad7f59bd5e694de1634bd5745561f8443733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Amines</topic><topic>Cross coupling</topic><topic>Glycine</topic><topic>Organic compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pan, Changduo</creatorcontrib><creatorcontrib>Chen, Dongdong</creatorcontrib><creatorcontrib>Cheng, Yangjian</creatorcontrib><creatorcontrib>Yu, Jin-Tao</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pan, Changduo</au><au>Chen, Dongdong</au><au>Cheng, Yangjian</au><au>Yu, Jin-Tao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photocatalytic redox-neutral α-C(sp 3 )-H pyridination of glycine derivatives and N -arylamines with cyanopyridines</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2024-04-18</date><risdate>2024</risdate><volume>60</volume><issue>33</issue><spage>4451</spage><epage>4454</epage><pages>4451-4454</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>A photo-induced α-C(sp
)-H decyanative pyridination of
-arylglycine derivatives with cyanopyridines was developed. This reaction was performed under organic photocatalytic and redox-neutral conditions
a radical-radical cross-coupling process. Besides, the protocol was also suitable for the C(sp
)-H pyridination of
-aryl tetrahydroisoquinolines as well as benzylamines.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>38563645</pmid><doi>10.1039/d4cc00906a</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-0264-9407</orcidid><orcidid>https://orcid.org/0000-0001-5878-3835</orcidid></addata></record> |
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| identifier | ISSN: 1359-7345 |
| ispartof | Chemical communications (Cambridge, England), 2024-04, Vol.60 (33), p.4451-4454 |
| issn | 1359-7345 1364-548X |
| language | eng |
| recordid | cdi_proquest_miscellaneous_3031135025 |
| source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| subjects | Amines Cross coupling Glycine Organic compounds |
| title | Photocatalytic redox-neutral α-C(sp 3 )-H pyridination of glycine derivatives and N -arylamines with cyanopyridines |
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