Direct carbon-carbon bond formation via soft enolization: aldol addition of alpha-halogenated thioesters

dc.contributor.author

Yost, Julianne M

dc.contributor.author

Alfie, Rachel J

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Tarsis, Emily M

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Chong, Insun

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Coltart, Don M

dc.date.accessioned

2011-06-21T17:27:17Z

dc.date.available

2011-06-21T17:27:17Z

dc.date.issued

2011

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.

dc.description.version

Version of Record

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.

dc.identifier.issn

1359-7345

dc.identifier.uri

https://hdl.handle.net/10161/4130

dc.language.iso

en_US

dc.publisher

Royal Society of Chemistry (RSC)

dc.relation.isversionof

10.1039/c0cc02345k

dc.relation.journal

Chemical Communications

dc.subject

darzens

dc.subject

acids

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triethylamine

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1,3-diketones

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condensation

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ketones

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facile

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esters

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chemistry, multidisciplinary

dc.title

Direct carbon-carbon bond formation via soft enolization: aldol addition of alpha-halogenated thioesters

dc.title.alternative
dc.type

Other article

duke.date.pubdate

2011-00-00

duke.description.issue

1

duke.description.volume

47

pubs.begin-page

571

pubs.end-page

572

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