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dc.contributor.author Yost, Julianne M. en_US
dc.contributor.author Alfie, Rachel J. en_US
dc.contributor.author Tarsis, Emily en_US
dc.contributor.author Chong, Insun en_US
dc.contributor.author Coltart, Dr Don en_US
dc.date.accessioned 2011-06-21T17:27:17Z
dc.date.available 2011-06-21T17:27:17Z
dc.date.issued 2011 en_US
dc.identifier.citation Yost,Julianne M.;Alfie,Rachel J.;Tarsis,Emily M.;Chong,Insun;Coltart,Don M.. 2011. Direct carbon-carbon bond formation via soft enolization: aldol addition of alpha-halogenated thioesters. Chemical Communications 47(1): 571-572. en_US
dc.identifier.issn 1359-7345 en_US
dc.identifier.uri http://hdl.handle.net/10161/4130
dc.description.abstract alpha-Halo thioesters undergo soft enolization and syn-selective direct aldol addition to aldehydes in the presence of MgBr2 center dot OEt2 and i-Pr2NEt to produce alpha-halo-beta-hydroxy thioesters. en_US
dc.language.iso en_US en_US
dc.publisher ROYAL SOC CHEMISTRY en_US
dc.relation.isversionof doi:10.1039/c0cc02345k en_US
dc.subject darzens en_US
dc.subject acids en_US
dc.subject triethylamine en_US
dc.subject 1,3-diketones en_US
dc.subject condensation en_US
dc.subject ketones en_US
dc.subject facile en_US
dc.subject esters en_US
dc.subject chemistry, multidisciplinary en_US
dc.title Direct carbon-carbon bond formation via soft enolization: aldol addition of alpha-halogenated thioesters en_US
dc.title.alternative en_US
dc.description.version Version of Record en_US
duke.date.pubdate 2011-00-00 en_US
duke.description.endpage 572 en_US
duke.description.issue 1 en_US
duke.description.startpage 571 en_US
duke.description.volume 47 en_US
dc.relation.journal Chemical Communications en_US

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