| 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 |