Journal article

Conjugate addition of nitrogen nucleophiles to an alpha,beta-unsaturated pyrrolidinone

Abstract:: The conjugate addition of nitrogen nucleophiles to α,β-unsaturated lactam 1b under very mild conditions occurs in good yield with high diastereoselectivity. Deprotection provides a simple access to β-aminopyrrolidinones in excellent overall yield.

Publication status:: Published

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APA Style

Chan, P., Cottrell, I., & Moloney, M. (1997). Conjugate addition of nitrogen nucleophiles to an alpha,beta-unsaturated pyrrolidinone. TETRAHEDRON LETTERS, 38(33), 5891–5894.

MLA Style

Chan, P, et al. “Conjugate Addition of Nitrogen Nucleophiles to an Alpha,Beta-Unsaturated Pyrrolidinone.” TETRAHEDRON LETTERS, vol. 38, no. 33, 1997, pp. 5891–94.

Chicago Style

Chan, P, I Cottrell, and M Moloney. 1997. “Conjugate Addition of Nitrogen Nucleophiles to an Alpha,Beta-Unsaturated Pyrrolidinone.” TETRAHEDRON LETTERS 38 (33): 5891–94.
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Publisher copy:: 10.1016/S0040-4039(97)01312-9

Authors

+ Chan, P More by this author

Role:: Author

+ Cottrell, I More by this author

Role:: Author

+ Moloney, M More by this author

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

Journal:: TETRAHEDRON LETTERS More from this journal
Volume:: 38
Issue:: 33
Pages:: 5891-5894
Publication date:: 1997-08-18
DOI:: 10.1016/S0040-4039(97)01312-9
ISSN:: 0040-4039

Language:: English
Pubs id:: pubs:45687
UUID:: uuid:edcbbd88-de64-4338-8fa6-8cda8de23288
Local pid:: pubs:45687
Source identifiers:: 45687
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_edcbbd88de6443388fa68cda8de23288

Terms of use

Copyright date:: 1997

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

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