Csp3–H Bond Functionalization of α-Bromo Ketones for the Synthesis of α-Keto Thioamides Using Elemental Sulfur
An efficient metal- and additive-free synthesis of α-keto thioamides has been developed via sulfur oxidation of the C sp 3–H bond of α-bromo ketones with amines. This environmentally friendly strategy made it possible to synthesize a wide series of α-keto thioamides with broad functional group toler...
Gespeichert in:
Veröffentlicht in: | Russian journal of organic chemistry 2022, Vol.58 (9), p.1260-1266 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1266 |
---|---|
container_issue | 9 |
container_start_page | 1260 |
container_title | Russian journal of organic chemistry |
container_volume | 58 |
creator | Tian, Haiying Guo, Fang Chen, Xiuling |
description | An efficient metal- and additive-free synthesis of α-keto thioamides has been developed via sulfur oxidation of the C
sp
3–H bond of α-bromo ketones with amines. This environmentally friendly strategy made it possible to synthesize a wide series of α-keto thioamides with broad functional group tolerance. |
doi_str_mv | 10.1134/S107042802209010X |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2731085495</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2731085495</sourcerecordid><originalsourceid>FETCH-LOGICAL-c161X-3d3b7ec8597c4bf08ddf2ca5b1583785da45251f8c806b9442a9207eeacd1d373</originalsourceid><addsrcrecordid>eNp1kE1Kw0AcxYMoWKsHcDfgOjqfzWRpS7ViwUVb6C5M5qNNSWfqTLKoK-_gSbyIh_AkTmjBhbj6P3i_9-D_kuQawVuECL2bIZhBijnEGOYQweVJ0kMDyFNCcnIadbTTzj9PLkLYQAgpoqSX-FHYke_3jwkYOqvAQ2tlUzkr6upNdAI4A74-06F3WweedeOsDsA4D5q1BrO9jSdU4Uh1PpivKye2lYrcIlR2Bca13mrbiBrM2tq0_jI5M6IO-up4-8niYTwfTdLpy-PT6H6aSjRAy5QoUmZacpZnkpYGcqUMloKViHGScaYEZZghwyWHgzKnFIscw0xrIRVSJCP95ObQu_PutdWhKTau9fG1UOCMIMgZzVmk0IGS3oXgtSl2vtoKvy8QLLppiz_Txgw-ZEJk7Ur73-b_Qz8WaH1F</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2731085495</pqid></control><display><type>article</type><title>Csp3–H Bond Functionalization of α-Bromo Ketones for the Synthesis of α-Keto Thioamides Using Elemental Sulfur</title><source>SpringerLink</source><creator>Tian, Haiying ; Guo, Fang ; Chen, Xiuling</creator><creatorcontrib>Tian, Haiying ; Guo, Fang ; Chen, Xiuling</creatorcontrib><description>An efficient metal- and additive-free synthesis of α-keto thioamides has been developed via sulfur oxidation of the C
sp
3–H bond of α-bromo ketones with amines. This environmentally friendly strategy made it possible to synthesize a wide series of α-keto thioamides with broad functional group tolerance.</description><identifier>ISSN: 1070-4280</identifier><identifier>EISSN: 1608-3393</identifier><identifier>DOI: 10.1134/S107042802209010X</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Amines ; Chemistry ; Chemistry and Materials Science ; Functional groups ; Hydrogen bonds ; Ketones ; Organic Chemistry ; Oxidation ; Sulfur ; Synthesis</subject><ispartof>Russian journal of organic chemistry, 2022, Vol.58 (9), p.1260-1266</ispartof><rights>Pleiades Publishing, Ltd. 2022</rights><rights>Pleiades Publishing, Ltd. 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c161X-3d3b7ec8597c4bf08ddf2ca5b1583785da45251f8c806b9442a9207eeacd1d373</citedby><cites>FETCH-LOGICAL-c161X-3d3b7ec8597c4bf08ddf2ca5b1583785da45251f8c806b9442a9207eeacd1d373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S107042802209010X$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S107042802209010X$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Tian, Haiying</creatorcontrib><creatorcontrib>Guo, Fang</creatorcontrib><creatorcontrib>Chen, Xiuling</creatorcontrib><title>Csp3–H Bond Functionalization of α-Bromo Ketones for the Synthesis of α-Keto Thioamides Using Elemental Sulfur</title><title>Russian journal of organic chemistry</title><addtitle>Russ J Org Chem</addtitle><description>An efficient metal- and additive-free synthesis of α-keto thioamides has been developed via sulfur oxidation of the C
sp
3–H bond of α-bromo ketones with amines. This environmentally friendly strategy made it possible to synthesize a wide series of α-keto thioamides with broad functional group tolerance.</description><subject>Amines</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Functional groups</subject><subject>Hydrogen bonds</subject><subject>Ketones</subject><subject>Organic Chemistry</subject><subject>Oxidation</subject><subject>Sulfur</subject><subject>Synthesis</subject><issn>1070-4280</issn><issn>1608-3393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kE1Kw0AcxYMoWKsHcDfgOjqfzWRpS7ViwUVb6C5M5qNNSWfqTLKoK-_gSbyIh_AkTmjBhbj6P3i_9-D_kuQawVuECL2bIZhBijnEGOYQweVJ0kMDyFNCcnIadbTTzj9PLkLYQAgpoqSX-FHYke_3jwkYOqvAQ2tlUzkr6upNdAI4A74-06F3WweedeOsDsA4D5q1BrO9jSdU4Uh1PpivKye2lYrcIlR2Bca13mrbiBrM2tq0_jI5M6IO-up4-8niYTwfTdLpy-PT6H6aSjRAy5QoUmZacpZnkpYGcqUMloKViHGScaYEZZghwyWHgzKnFIscw0xrIRVSJCP95ObQu_PutdWhKTau9fG1UOCMIMgZzVmk0IGS3oXgtSl2vtoKvy8QLLppiz_Txgw-ZEJk7Ur73-b_Qz8WaH1F</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Tian, Haiying</creator><creator>Guo, Fang</creator><creator>Chen, Xiuling</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2022</creationdate><title>Csp3–H Bond Functionalization of α-Bromo Ketones for the Synthesis of α-Keto Thioamides Using Elemental Sulfur</title><author>Tian, Haiying ; Guo, Fang ; Chen, Xiuling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c161X-3d3b7ec8597c4bf08ddf2ca5b1583785da45251f8c806b9442a9207eeacd1d373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Amines</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Functional groups</topic><topic>Hydrogen bonds</topic><topic>Ketones</topic><topic>Organic Chemistry</topic><topic>Oxidation</topic><topic>Sulfur</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tian, Haiying</creatorcontrib><creatorcontrib>Guo, Fang</creatorcontrib><creatorcontrib>Chen, Xiuling</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tian, Haiying</au><au>Guo, Fang</au><au>Chen, Xiuling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Csp3–H Bond Functionalization of α-Bromo Ketones for the Synthesis of α-Keto Thioamides Using Elemental Sulfur</atitle><jtitle>Russian journal of organic chemistry</jtitle><stitle>Russ J Org Chem</stitle><date>2022</date><risdate>2022</risdate><volume>58</volume><issue>9</issue><spage>1260</spage><epage>1266</epage><pages>1260-1266</pages><issn>1070-4280</issn><eissn>1608-3393</eissn><abstract>An efficient metal- and additive-free synthesis of α-keto thioamides has been developed via sulfur oxidation of the C
sp
3–H bond of α-bromo ketones with amines. This environmentally friendly strategy made it possible to synthesize a wide series of α-keto thioamides with broad functional group tolerance.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S107042802209010X</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1070-4280 |
ispartof | Russian journal of organic chemistry, 2022, Vol.58 (9), p.1260-1266 |
issn | 1070-4280 1608-3393 |
language | eng |
recordid | cdi_proquest_journals_2731085495 |
source | SpringerLink |
subjects | Amines Chemistry Chemistry and Materials Science Functional groups Hydrogen bonds Ketones Organic Chemistry Oxidation Sulfur Synthesis |
title | Csp3–H Bond Functionalization of α-Bromo Ketones for the Synthesis of α-Keto Thioamides Using Elemental Sulfur |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T16%3A28%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Csp3%E2%80%93H%20Bond%20Functionalization%20of%20%CE%B1-Bromo%20Ketones%20for%20the%20Synthesis%20of%20%CE%B1-Keto%20Thioamides%20Using%20Elemental%20Sulfur&rft.jtitle=Russian%20journal%20of%20organic%20chemistry&rft.au=Tian,%20Haiying&rft.date=2022&rft.volume=58&rft.issue=9&rft.spage=1260&rft.epage=1266&rft.pages=1260-1266&rft.issn=1070-4280&rft.eissn=1608-3393&rft_id=info:doi/10.1134/S107042802209010X&rft_dat=%3Cproquest_cross%3E2731085495%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2731085495&rft_id=info:pmid/&rfr_iscdi=true |