N-Heterocyclic carbene catalyzed synthesis of oxime estersElectronic supplementary information (ESI) available: Experimental procedures and full spectroscopic data for all isolated compounds. See DOI: 10.1039/c2ob26974k
A triazolium salt derived N -heterocyclic carbene catalyzes the redox esterification reaction between α-β-unsaturated aldehydes and oximes. The resulting saturated oxime esters were obtained in very good yields for a broad range of aliphatic, aromatic and heteroaromatic substrates. A selective, redo...
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| creator | Enders, Dieter Grossmann, André Van Craen, David |
| description | A triazolium salt derived
N
-heterocyclic carbene catalyzes the redox esterification reaction between α-β-unsaturated aldehydes and oximes. The resulting saturated oxime esters were obtained in very good yields for a broad range of aliphatic, aromatic and heteroaromatic substrates.
A selective, redox- and atom economical synthesis of oxime esters
via N
-heterocyclic carbene catalyzed redox esterification has been developed. The new protocol opens a convenient and direct entry to the title compounds in very high yields without any significant limitations in the substrate scope. |
| doi_str_mv | 10.1039/c2ob26974k |
| format | Article |
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-heterocyclic carbene catalyzes the redox esterification reaction between α-β-unsaturated aldehydes and oximes. The resulting saturated oxime esters were obtained in very good yields for a broad range of aliphatic, aromatic and heteroaromatic substrates.
A selective, redox- and atom economical synthesis of oxime esters
via N
-heterocyclic carbene catalyzed redox esterification has been developed. The new protocol opens a convenient and direct entry to the title compounds in very high yields without any significant limitations in the substrate scope.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/c2ob26974k</identifier><language>eng</language><creationdate>2013-01</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Enders, Dieter</creatorcontrib><creatorcontrib>Grossmann, André</creatorcontrib><creatorcontrib>Van Craen, David</creatorcontrib><title>N-Heterocyclic carbene catalyzed synthesis of oxime estersElectronic supplementary information (ESI) available: Experimental procedures and full spectroscopic data for all isolated compounds. See DOI: 10.1039/c2ob26974k</title><description>A triazolium salt derived
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A selective, redox- and atom economical synthesis of oxime esters
via N
-heterocyclic carbene catalyzed redox esterification has been developed. The new protocol opens a convenient and direct entry to the title compounds in very high yields without any significant limitations in the substrate scope.</description><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFkD1PwzAQhi0EEqWwsCMdGwwtzgeN0hWC2gWGskeOcxEGx7Z8Dmr4q_yZWhWCAQmmO-n9uEfH2HnC5wnPyhuZ2iZdlEX-dsAmSV4UM36blYffe8qP2QnRK-dJWSzyCft8nK0woLdylFpJkMI3aDDOIPT4gS3QaMILkiKwHdit6hGQYoIqjTJ4a2KKBuc09miC8CMo01nfi6Csgatqs74G8S6UFo3GJVRbh17trRpcvIvt4JFAmBa6QWsgt68laV1sbiMHxDoQUVJktQiRSdre2cG0NIcNItw_rZfw-wWn7KgTmvDsa07ZxUP1fLeaeZK1ixARtv6xZ1N2-Zdeu7bL_uvYAQ4ofnM</recordid><startdate>20130107</startdate><enddate>20130107</enddate><creator>Enders, Dieter</creator><creator>Grossmann, André</creator><creator>Van Craen, David</creator><scope/></search><sort><creationdate>20130107</creationdate><title>N-Heterocyclic carbene catalyzed synthesis of oxime estersElectronic supplementary information (ESI) available: Experimental procedures and full spectroscopic data for all isolated compounds. See DOI: 10.1039/c2ob26974k</title><author>Enders, Dieter ; Grossmann, André ; Van Craen, David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c2ob26974k3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Enders, Dieter</creatorcontrib><creatorcontrib>Grossmann, André</creatorcontrib><creatorcontrib>Van Craen, David</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Enders, Dieter</au><au>Grossmann, André</au><au>Van Craen, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>N-Heterocyclic carbene catalyzed synthesis of oxime estersElectronic supplementary information (ESI) available: Experimental procedures and full spectroscopic data for all isolated compounds. See DOI: 10.1039/c2ob26974k</atitle><date>2013-01-07</date><risdate>2013</risdate><volume>11</volume><issue>1</issue><spage>138</spage><epage>141</epage><pages>138-141</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>A triazolium salt derived
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A selective, redox- and atom economical synthesis of oxime esters
via N
-heterocyclic carbene catalyzed redox esterification has been developed. The new protocol opens a convenient and direct entry to the title compounds in very high yields without any significant limitations in the substrate scope.</abstract><doi>10.1039/c2ob26974k</doi><tpages>4</tpages></addata></record> |
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| source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| title | N-Heterocyclic carbene catalyzed synthesis of oxime estersElectronic supplementary information (ESI) available: Experimental procedures and full spectroscopic data for all isolated compounds. See DOI: 10.1039/c2ob26974k |
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