Journal article

Enantioselective organocatalytic Michael additions to acrylic acid derivatives: generation of all-carbon quaternary stereocentres.

Abstract:: Acrylic esters, thioesters and N-acryloyl pyrrole have been identified as effective electrophiles in the enantioselective Michael addition reaction with beta-keto ester pro-nucleophiles catalysed by a cinchona alkaloid derived bifunctional organocatalyst; enantiomeric excesses of up to 98% and yields of up to 96% can be obtained for a range of Michael acceptors and pro-nucleophiles.

Publication status:: Published

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APA Style

Rigby, C., & Dixon, D. (2008). Enantioselective organocatalytic Michael additions to acrylic acid derivatives: generation of all-carbon quaternary stereocentres. Chemical Communications, 32, 3798–3800.

MLA Style

Rigby, C, and D Dixon. “Enantioselective Organocatalytic Michael Additions to Acrylic Acid Derivatives: Generation of All-Carbon Quaternary Stereocentres.” Chemical Communications, no. 32, 2008, pp. 3798–800.

Chicago Style

Rigby, C, and D Dixon. 2008. “Enantioselective Organocatalytic Michael Additions to Acrylic Acid Derivatives: Generation of All-Carbon Quaternary Stereocentres.” Chemical Communications, no. 32: 3798–3800.
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Publisher copy:: 10.1039/b805233f

Authors

+ Rigby, C More by this author

Role:: Author

+ Dixon, D More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

Journal:: Chemical Communications More from this journal
Issue:: 32
Pages:: 3798-3800
Publication date:: 2008-08-01
DOI:: 10.1039/b805233f
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Pubs id:: pubs:34342
UUID:: uuid:0715a1e7-6ede-4e18-8654-95ba16fddd3b
Local pid:: pubs:34342
Source identifiers:: 34342
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_0715a1e76ede4e18865495ba16fddd3b

Terms of use

Copyright date:: 2008

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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