Journal article

Pyrrolidinones derived from (S)-pyroglutamic acid. Part 4. alpha,beta-diaminopyrrolidinones

Abstract:: The electrophilic amination of a β-aminolactam, itself derived from the conjugate addition of O,N-dibenzyl-hydroxylamine to a highly activated α, β-unsaturated bicyclic lactam, provides direct access to conformationally constrained diamines. Sequential deprotection allows the synthesis of 3,4-diaminopyroglutaminols.

Publication status:: Published

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APA Style

Chan, P., Cottrell, I., & Moloney, M. (2001). Pyrrolidinones derived from (S)-pyroglutamic acid. Part 4. alpha,beta-diaminopyrrolidinones. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 22, 3007–3012.

MLA Style

Chan, P., et al. “Pyrrolidinones Derived from (S)-Pyroglutamic Acid. Part 4. Alpha,Beta-Diaminopyrrolidinones.” JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, no. 22, 2001, pp. 3007–12.

Chicago Style

Chan, P, I Cottrell, and M Moloney. 2001. “Pyrrolidinones Derived from (S)-Pyroglutamic Acid. Part 4. Alpha,Beta-Diaminopyrrolidinones.” JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, no. 22: 3007–12.
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Publisher copy:: 10.1039/b106783b

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:: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 More from this journal
Issue:: 22
Pages:: 3007-3012
Publication date:: 2001-01-01
DOI:: 10.1039/b106783b
EISSN:: 1364-5463
ISSN:: 1472-7781

Language:: English
Pubs id:: pubs:38045
UUID:: uuid:99f1c325-006b-4b12-8ac9-aaff4d2250f0
Local pid:: pubs:38045
Source identifiers:: 38045
Deposit date:: 2012-12-19

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Copyright date:: 2001

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

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