Taming the Carboxyl Group for Directed Carbometalation: Observations on the Use of Anions, Dianions and Ester Enolates. Issue 29 (24th June 2014)

Record Type:: Journal Article
Title:: Taming the Carboxyl Group for Directed Carbometalation: Observations on the Use of Anions, Dianions and Ester Enolates. Issue 29 (24th June 2014)
Main Title:: Taming the Carboxyl Group for Directed Carbometalation: Observations on the Use of Anions, Dianions and Ester Enolates
Authors:: Desrat, Sandy
Gray, Philip J.
Penny, Matthew R.
Motherwell, William B.
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Carboxylate anions, dianions and ester enolates provide simultaneous protection and activation for directed carbometalation reactions. Advantage can be taken of the bis‐carbanionic character of the intermediate for further controlled CC bond forming reactions.</p> </abstract>
Is Part Of:: Chemistry. Volume 20:Issue 29(2014)
Journal:: Chemistry
Issue:: Volume 20:Issue 29(2014)
Issue Display:: Volume 20, Issue 29 (2014)
Year:: 2014
Volume:: 20
Issue:: 29
Issue Sort Value:: 2014-0020-0029-0000
Page Start:: 8918
Page End:: 8922
Publication Date:: 2014-06-24
Subjects:: Chemistry -- Periodicals
540
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/chem.201403294 ↗
Languages:: English
ISSNs:: 0947-6539
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
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Ingest File:: 3297.xml