Journal article

Exerting control over the acyloin reaction.

Abstract:: A synthetic method for conducting the acyloin reaction using electron transfer in solution is reported. By linking two esters via their oxygen atoms, it was possible to perform crossed acyloin reactions between two different ester functionalities and display a high degree of preference for an intramolecular coupling process.

Publication status:: Published

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APA Style

Donohoe, T., Jahanshahi, A., Tucker, M., Bhatti, F., Roslan, I., Kabeshov, M., & Wrigley, G. (2011). Exerting control over the acyloin reaction. Chemical Communications, 47(20), 5849–5851.

MLA Style

Donohoe, T., et al. “Exerting Control over the Acyloin Reaction.” Chemical Communications, vol. 47, no. 20, 2011, pp. 5849–51.

Chicago Style

Donohoe, T, A Jahanshahi, M Tucker, F Bhatti, I Roslan, M Kabeshov, and G Wrigley. 2011. “Exerting Control over the Acyloin Reaction.” Chemical Communications 47 (20): 5849–51.
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Publisher copy:: 10.1039/c1cc11654a

Authors

+ Donohoe, T More by this author

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

+ Jahanshahi, A More by this author

Role:: Author

+ Tucker, M More by this author

Role:: Author

+ Bhatti, F More by this author

Role:: Author

+ Roslan, I More by this author

Role:: Author

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Journal:: Chemical Communications More from this journal
Volume:: 47
Issue:: 20
Pages:: 5849-5851
Publication date:: 2011-05-01
DOI:: 10.1039/c1cc11654a
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Keywords:: Electron Transport

Stereoisomerism

Lithium

Fatty Alcohols

Esters
Pubs id:: pubs:134963
UUID:: uuid:1873f03b-a8f5-4a1a-ae89-8b4f3679310d
Local pid:: pubs:134963
Source identifiers:: 134963
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2011

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

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