Journal article

Functionalised pyrrolidinones by conjugate addition of stabilised enolates and reformatsky reagents

Abstract:: The α,β-unsaturated lactam 1b has been found to readily undergo conjugate addition reactions with a range of stabilised carbon nucleophiles and Reformatsky reagents under mild conditions in good yield with high diastereoselectivity. This method provides a simple and versatile approach to highly functionalised pyrrolidinones.

Publication status:: Published

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APA Style

Dyer, J., Keeling, S., & Moloney, M. (1996). Functionalised pyrrolidinones by conjugate addition of stabilised enolates and reformatsky reagents. TETRAHEDRON LETTERS, 37(26), 4573–4576.

MLA Style

Dyer, J, et al. “Functionalised Pyrrolidinones by Conjugate Addition of Stabilised Enolates and Reformatsky Reagents.” TETRAHEDRON LETTERS, vol. 37, no. 26, 1996, pp. 4573–76.

Chicago Style

Dyer, J, S Keeling, and M Moloney. 1996. “Functionalised Pyrrolidinones by Conjugate Addition of Stabilised Enolates and Reformatsky Reagents.” TETRAHEDRON LETTERS 37 (26): 4573–76.
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Publisher copy:: 10.1016/0040-4039(96)00849-0

Authors

+ Dyer, J More by this author

Role:: Author

+ Keeling, S 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:: 37
Issue:: 26
Pages:: 4573-4576
Publication date:: 1996-06-24
DOI:: 10.1016/0040-4039(96)00849-0
ISSN:: 0040-4039

Language:: English
Pubs id:: pubs:45243
UUID:: uuid:eb19541f-c78f-475d-a264-eae3778bf29f
Local pid:: pubs:45243
Source identifiers:: 45243
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_eb19541fc78f475da264eae3778bf29f

Terms of use

Copyright date:: 1996

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

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