Journal article

Enantiopure oxazolidinones as chiral acids in the asymmetric protonation of N-Boc pyrrole derived enolates.

Abstract:: The first use of geminally disubstituted oxazolidinones as chiral protonating agents is described: these new acids are able to directly protonate an enolate generated by the ammonia free partial reduction of an electron deficient pyrrole and give up to 68% ee in the pyrroline product.

Publication status:: Published

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APA Style

Carbery, D. R., & Donohoe, T. (2004). Enantiopure oxazolidinones as chiral acids in the asymmetric protonation of N-Boc pyrrole derived enolates. Chemical Communications, 10(6), 722–723.

MLA Style

Carbery, D. R., and T. Donohoe. “Enantiopure Oxazolidinones as Chiral Acids in the Asymmetric Protonation of N-Boc Pyrrole Derived Enolates.” Chemical Communications, vol. 10, no. 6, 2004, pp. 722–23.

Chicago Style

Carbery, DR, and T Donohoe. 2004. “Enantiopure Oxazolidinones as Chiral Acids in the Asymmetric Protonation of N-Boc Pyrrole Derived Enolates.” Chemical Communications 10 (6): 722–23.
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Publisher copy:: 10.1039/b316719d

Authors

+ Carbery, DR More by this author

Role:: Author

+ Donohoe, T 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
Volume:: 10
Issue:: 6
Pages:: 722-723
Publication date:: 2004-03-01
DOI:: 10.1039/b316719d
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Pubs id:: pubs:32653
UUID:: uuid:ad0836d0-6097-4240-a649-18f5b1a484af
Local pid:: pubs:32653
Source identifiers:: 32653
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2004

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

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