Journal article

N-acyl 'Quat' pyrrolidinone auxiliary as a chiral amide equivalent via direct aminolysis

Abstract:: A novel route into chiral amides is achieved through the efficient, non-racemising, cleavage of N-acyl side chains from a 'Quat' pyrrolidinone chiral auxiliary using a range of N-nucleophiles.

Publication status:: Published

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APA Style

Davies, S., & Dixon, D. (1998). N-acyl 'Quat' pyrrolidinone auxiliary as a chiral amide equivalent via direct aminolysis. SYNLETT, 9, 963-+.

MLA Style

Davies, S, and D Dixon. “N-Acyl 'Quat' Pyrrolidinone Auxiliary as a Chiral Amide Equivalent via Direct Aminolysis.” SYNLETT, no. 9, 1998, pp. 963-+.

Chicago Style

Davies, S, and D Dixon. 1998. “N-Acyl 'Quat' Pyrrolidinone Auxiliary as a Chiral Amide Equivalent via Direct Aminolysis.” SYNLETT, no. 9: 963-+.
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Publisher copy:: 10.1055/s-1998-1839

Authors

+ Davies, S More by this author

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

+ Dixon, D More by this author

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

Journal:: SYNLETT More from this journal
Issue:: 9
Pages:: 963-+
Publication date:: 1998-09-01
DOI:: 10.1055/s-1998-1839
ISSN:: 0936-5214

Language:: English
Keywords:: aminolysis

'Quat' chiral auxiliary

amides
Pubs id:: pubs:36727
UUID:: uuid:09979f06-7dac-475b-8783-7fb4a0b5e532
Local pid:: pubs:36727
Source identifiers:: 36727
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_09979f067dac475b87837fb4a0b5e532

Terms of use

Copyright date:: 1998

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

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