O- and C-alkylations of ethyl nitroacetate with benzyl halides
THE chemistry of nitronic esters remains relatively unknown due to their conspicuous feature ofinstability. In the preceding papers, we described the late progress in the researchof nitronic esters: (i) nitronic esters were first synthesized via O-alkylation of the alkali met-
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| Veröffentlicht in: | Chinese science bulletin 1997-10, Vol.42 (19), p.1628-1631 |
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| container_end_page | 1631 |
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| container_issue | 19 |
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| container_title | Chinese science bulletin |
| container_volume | 42 |
| creator | Kang, Fu’an Yin, Hongyi Yin, Chenglie |
| description | THE chemistry of nitronic esters remains relatively unknown due to their conspicuous feature ofinstability. In the preceding papers, we described the late progress in the researchof nitronic esters: (i) nitronic esters were first synthesized via O-alkylation of the alkali met- |
| doi_str_mv | 10.1007/BF02882573 |
| format | Article |
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In the preceding papers, we described the late progress in the researchof nitronic esters: (i) nitronic esters were first synthesized via O-alkylation of the alkali met-</description><identifier>ISSN: 1001-6538</identifier><identifier>ISSN: 2095-9273</identifier><identifier>EISSN: 1861-9541</identifier><identifier>EISSN: 2095-9281</identifier><identifier>DOI: 10.1007/BF02882573</identifier><language>eng</language><publisher>Beijing: Springer Nature B.V</publisher><subject>Alkylation ; benzyl ; C-alkylation ; ethyl ; Halides ; nitroacetate ; O-alkylation</subject><ispartof>Chinese science bulletin, 1997-10, Vol.42 (19), p.1628-1631</ispartof><rights>Science in China Press 1997.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c285t-5cebf7b88aa1a3ac8ee29dde1a831b881b102e6d0d5eb09a2953b2889fb5d70b3</citedby><cites>FETCH-LOGICAL-c285t-5cebf7b88aa1a3ac8ee29dde1a831b881b102e6d0d5eb09a2953b2889fb5d70b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/86894X/86894X.jpg</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Kang, Fu’an</creatorcontrib><creatorcontrib>Yin, Hongyi</creatorcontrib><creatorcontrib>Yin, Chenglie</creatorcontrib><title>O- and C-alkylations of ethyl nitroacetate with benzyl halides</title><title>Chinese science bulletin</title><addtitle>Chinese Science Bulletin</addtitle><description>THE chemistry of nitronic esters remains relatively unknown due to their conspicuous feature ofinstability. In the preceding papers, we described the late progress in the researchof nitronic esters: (i) nitronic esters were first synthesized via O-alkylation of the alkali met-</description><subject>Alkylation</subject><subject>benzyl</subject><subject>C-alkylation</subject><subject>ethyl</subject><subject>Halides</subject><subject>nitroacetate</subject><subject>O-alkylation</subject><issn>1001-6538</issn><issn>2095-9273</issn><issn>1861-9541</issn><issn>2095-9281</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNpFkM1KAzEUhYMoWKsbnyDgTojeJGYmsxG0WBUK3eh6SCaZztQxaZMUGZ_eSMWu7t_HOdyD0CWFGwpQ3j7OgUnJRMmP0ITKgpJK3NHj3ANQUgguT9FZjOs8cVqyCbpfEqycwTOiho9xUKn3LmLfYpu6ccCuT8GrxiaVLP7qU4e1dd_50KmhNzaeo5NWDdFe_NUpep8_vc1eyGL5_Dp7WJCGSZGIaKxuSy2lUlRx1UhrWWWMpUpymtdUU2C2MGCE1VApVgmu8yNVq4UpQfMputrrboLf7mxM9drvgsuWNStlUXEJXGbqek81wccYbFtvQv-pwlhTqH_zqQ_5HCSbzrvVtnerf5rneIAKAM5_AO_qYmA</recordid><startdate>19971001</startdate><enddate>19971001</enddate><creator>Kang, Fu’an</creator><creator>Yin, Hongyi</creator><creator>Yin, Chenglie</creator><general>Springer Nature B.V</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>~WA</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19971001</creationdate><title>O- and C-alkylations of ethyl nitroacetate with benzyl halides</title><author>Kang, Fu’an ; Yin, Hongyi ; Yin, Chenglie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c285t-5cebf7b88aa1a3ac8ee29dde1a831b881b102e6d0d5eb09a2953b2889fb5d70b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Alkylation</topic><topic>benzyl</topic><topic>C-alkylation</topic><topic>ethyl</topic><topic>Halides</topic><topic>nitroacetate</topic><topic>O-alkylation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kang, Fu’an</creatorcontrib><creatorcontrib>Yin, Hongyi</creatorcontrib><creatorcontrib>Yin, Chenglie</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>维普中文期刊数据库</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>CrossRef</collection><jtitle>Chinese science bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kang, Fu’an</au><au>Yin, Hongyi</au><au>Yin, Chenglie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>O- and C-alkylations of ethyl nitroacetate with benzyl halides</atitle><jtitle>Chinese science bulletin</jtitle><addtitle>Chinese Science Bulletin</addtitle><date>1997-10-01</date><risdate>1997</risdate><volume>42</volume><issue>19</issue><spage>1628</spage><epage>1631</epage><pages>1628-1631</pages><issn>1001-6538</issn><issn>2095-9273</issn><eissn>1861-9541</eissn><eissn>2095-9281</eissn><abstract>THE chemistry of nitronic esters remains relatively unknown due to their conspicuous feature ofinstability. In the preceding papers, we described the late progress in the researchof nitronic esters: (i) nitronic esters were first synthesized via O-alkylation of the alkali met-</abstract><cop>Beijing</cop><pub>Springer Nature B.V</pub><doi>10.1007/BF02882573</doi><tpages>4</tpages></addata></record> |
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| identifier | ISSN: 1001-6538 |
| ispartof | Chinese science bulletin, 1997-10, Vol.42 (19), p.1628-1631 |
| issn | 1001-6538 2095-9273 1861-9541 2095-9281 |
| language | eng |
| recordid | cdi_proquest_journals_2786938038 |
| source | Alma/SFX Local Collection |
| subjects | Alkylation benzyl C-alkylation ethyl Halides nitroacetate O-alkylation |
| title | O- and C-alkylations of ethyl nitroacetate with benzyl halides |
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