Journal article

Pyrrolidinones derived from (S)-pyroglutamic acid. Part 2. Conformationally constrained kainoid analogues

Abstract:: Novel conformationally constrained glutamate analogues are readily available from (S)-pyroglutamic acid using a bicyclic lactam as a synthetic template; diastereocontrolled modification of the pyrrolidine ring using a sequential conjugate addition-substitution strategy permits access to several kainoid analogues in a versatile strategy. The pyrrolidinone ring conformation appears to be controllable by the nature of remote substituents on the heterocyclic ring. © The Royal Society of Chemistry 2000.

Publication status:: Published

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APA Style

Dyer, J., King, A., Keeling, S., & Moloney, M. (2000). Pyrrolidinones derived from (S)-pyroglutamic acid. Part 2. Conformationally constrained kainoid analogues. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 16, 2793–2804.

MLA Style

Dyer, J., et al. “Pyrrolidinones Derived from (S)-Pyroglutamic Acid. Part 2. Conformationally Constrained Kainoid Analogues.” JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, no. 16, 2000, pp. 2793–804.

Chicago Style

Dyer, J, A King, S Keeling, and M Moloney. 2000. “Pyrrolidinones Derived from (S)-Pyroglutamic Acid. Part 2. Conformationally Constrained Kainoid Analogues.” JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, no. 16: 2793–2804.
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Publisher copy:: 10.1039/b002001j

Authors

+ Dyer, J More by this author

Role:: Author

+ King, A 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:: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 More from this journal
Issue:: 16
Pages:: 2793-2804
Publication date:: 2000-01-01
DOI:: 10.1039/b002001j
EISSN:: 1364-5463
ISSN:: 1470-4358

Language:: English
Pubs id:: pubs:37529
UUID:: uuid:38831d00-bc92-4a4c-81fa-c2040fa5dee5
Local pid:: pubs:37529
Source identifiers:: 37529
Deposit date:: 2012-12-19

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Copyright date:: 2000

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

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