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Electrochemical Synthesis of 5‐Selenouracil Derivatives by Selenylation of Uracils
A simple and efficient electrochemical selenylation of uracils in the presence of NH4I for the synthesis of 5‐selenouracils has been developed. This transformation was performed in the transition metal‐free, oxidant‐free, and aerobic conditions, providing a rapid and practical protocol to 5‐selenour...
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Published in: | European journal of organic chemistry 2020-08, Vol.2020 (28), p.4384-4388 |
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container_end_page | 4388 |
container_issue | 28 |
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container_title | European journal of organic chemistry |
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creator | Wang, Qian Ma, Xian‐Li Chen, Yan‐Yan Jiang, Cai‐Na Xu, Yan‐Li |
description | A simple and efficient electrochemical selenylation of uracils in the presence of NH4I for the synthesis of 5‐selenouracils has been developed. This transformation was performed in the transition metal‐free, oxidant‐free, and aerobic conditions, providing a rapid and practical protocol to 5‐selenouracil derivatives.
A simple and efficient electrochemical selenylation of uracils in the presence of NH4I for the synthesis of 5‐selenouracils has been developed. This transformation was performed in the transition metal‐free, oxidant‐free, and air conditions, providing a rapid and practical protocol to 5‐selenouracil derivatives. |
doi_str_mv | 10.1002/ejoc.202000637 |
format | article |
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A simple and efficient electrochemical selenylation of uracils in the presence of NH4I for the synthesis of 5‐selenouracils has been developed. This transformation was performed in the transition metal‐free, oxidant‐free, and air conditions, providing a rapid and practical protocol to 5‐selenouracil derivatives.</description><identifier>ISSN: 1434-193X</identifier><identifier>EISSN: 1099-0690</identifier><identifier>DOI: 10.1002/ejoc.202000637</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Chemical synthesis ; Derivatives ; Electrochemistry ; Nucleobases ; Oxidizing agents ; Selenium ; Synthetic methods ; Transition metals ; Uracil</subject><ispartof>European journal of organic chemistry, 2020-08, Vol.2020 (28), p.4384-4388</ispartof><rights>2020 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3837-bba407ee22736ef4aeb4ccfdc24f47c969d074d8e8b3bc6146bd7744c976033</citedby><cites>FETCH-LOGICAL-c3837-bba407ee22736ef4aeb4ccfdc24f47c969d074d8e8b3bc6146bd7744c976033</cites><orcidid>0000-0003-1373-6431</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Wang, Qian</creatorcontrib><creatorcontrib>Ma, Xian‐Li</creatorcontrib><creatorcontrib>Chen, Yan‐Yan</creatorcontrib><creatorcontrib>Jiang, Cai‐Na</creatorcontrib><creatorcontrib>Xu, Yan‐Li</creatorcontrib><title>Electrochemical Synthesis of 5‐Selenouracil Derivatives by Selenylation of Uracils</title><title>European journal of organic chemistry</title><description>A simple and efficient electrochemical selenylation of uracils in the presence of NH4I for the synthesis of 5‐selenouracils has been developed. This transformation was performed in the transition metal‐free, oxidant‐free, and aerobic conditions, providing a rapid and practical protocol to 5‐selenouracil derivatives.
A simple and efficient electrochemical selenylation of uracils in the presence of NH4I for the synthesis of 5‐selenouracils has been developed. This transformation was performed in the transition metal‐free, oxidant‐free, and air conditions, providing a rapid and practical protocol to 5‐selenouracil derivatives.</description><subject>Chemical synthesis</subject><subject>Derivatives</subject><subject>Electrochemistry</subject><subject>Nucleobases</subject><subject>Oxidizing agents</subject><subject>Selenium</subject><subject>Synthetic methods</subject><subject>Transition metals</subject><subject>Uracil</subject><issn>1434-193X</issn><issn>1099-0690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0EEqWwZR2JdYpf2PESlfJSpS5SJHaW40xUV2lc7LQoOz6Bb-RLSFsES1Yzmjl37ugidEnwiGBMr2Hp7YhiijEWTB6hAcFKpVgofNz3nPGUKPZ6is5iXPaMEoIM0HxSg22DtwtYOWvqJO-adgHRxcRXyc3Xx2cONTR-E4x1dXIHwW1N67YQk6JL9ruu7ge-2fEveyqeo5PK1BEufuoQ5feT-fgxnc4ensa309SyjMm0KAzHEoBSyQRU3EDBra1KS3nFpVVClVjyMoOsYIUVhIuilJJzq6TAjA3R1eHqOvi3DcRWL_s3m95QU04zxRShtKdGB8oGH2OASq-DW5nQaYL1Lje9y03_5tYL1EHw7mro_qH15Hk2_tN-A9rec7M</recordid><startdate>20200802</startdate><enddate>20200802</enddate><creator>Wang, Qian</creator><creator>Ma, Xian‐Li</creator><creator>Chen, Yan‐Yan</creator><creator>Jiang, Cai‐Na</creator><creator>Xu, Yan‐Li</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-1373-6431</orcidid></search><sort><creationdate>20200802</creationdate><title>Electrochemical Synthesis of 5‐Selenouracil Derivatives by Selenylation of Uracils</title><author>Wang, Qian ; Ma, Xian‐Li ; Chen, Yan‐Yan ; Jiang, Cai‐Na ; Xu, Yan‐Li</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3837-bba407ee22736ef4aeb4ccfdc24f47c969d074d8e8b3bc6146bd7744c976033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Chemical synthesis</topic><topic>Derivatives</topic><topic>Electrochemistry</topic><topic>Nucleobases</topic><topic>Oxidizing agents</topic><topic>Selenium</topic><topic>Synthetic methods</topic><topic>Transition metals</topic><topic>Uracil</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Qian</creatorcontrib><creatorcontrib>Ma, Xian‐Li</creatorcontrib><creatorcontrib>Chen, Yan‐Yan</creatorcontrib><creatorcontrib>Jiang, Cai‐Na</creatorcontrib><creatorcontrib>Xu, Yan‐Li</creatorcontrib><collection>CrossRef</collection><jtitle>European journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Qian</au><au>Ma, Xian‐Li</au><au>Chen, Yan‐Yan</au><au>Jiang, Cai‐Na</au><au>Xu, Yan‐Li</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemical Synthesis of 5‐Selenouracil Derivatives by Selenylation of Uracils</atitle><jtitle>European journal of organic chemistry</jtitle><date>2020-08-02</date><risdate>2020</risdate><volume>2020</volume><issue>28</issue><spage>4384</spage><epage>4388</epage><pages>4384-4388</pages><issn>1434-193X</issn><eissn>1099-0690</eissn><abstract>A simple and efficient electrochemical selenylation of uracils in the presence of NH4I for the synthesis of 5‐selenouracils has been developed. This transformation was performed in the transition metal‐free, oxidant‐free, and aerobic conditions, providing a rapid and practical protocol to 5‐selenouracil derivatives.
A simple and efficient electrochemical selenylation of uracils in the presence of NH4I for the synthesis of 5‐selenouracils has been developed. This transformation was performed in the transition metal‐free, oxidant‐free, and air conditions, providing a rapid and practical protocol to 5‐selenouracil derivatives.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ejoc.202000637</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-1373-6431</orcidid></addata></record> |
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subjects | Chemical synthesis Derivatives Electrochemistry Nucleobases Oxidizing agents Selenium Synthetic methods Transition metals Uracil |
title | Electrochemical Synthesis of 5‐Selenouracil Derivatives by Selenylation of Uracils |
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