Journal article

Efficient enantioselective synthesis of tetramic acids and lactams from threonine

Abstract:: Regioselective Dieckmann and aldol cyclisations using an N-acyloxazolidine derived from threonine give substituted tetramic acids and pyroglutamates in high yield and enantioselectivity. These are easily deprotected under mild conditions to give products, some of which exhibit antibacterial activity. © 2007 Elsevier Ltd. All rights reserved.

Publication status:: Published

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APA Style

Anwar, M., & Moloney, M. (2007). Efficient enantioselective synthesis of tetramic acids and lactams from threonine. TETRAHEDRON LETTERS, 48(41), 7259–7262.

MLA Style

Anwar, M, and M Moloney. “Efficient Enantioselective Synthesis of Tetramic Acids and Lactams from Threonine.” TETRAHEDRON LETTERS, vol. 48, no. 41, 2007, pp. 7259–62.

Chicago Style

Anwar, M, and M Moloney. 2007. “Efficient Enantioselective Synthesis of Tetramic Acids and Lactams from Threonine.” TETRAHEDRON LETTERS 48 (41): 7259–62.
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Publisher copy:: 10.1016/j.tetlet.2007.08.052

Authors

+ Anwar, M 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:: 48
Issue:: 41
Pages:: 7259-7262
Publication date:: 2007-10-08
DOI:: 10.1016/j.tetlet.2007.08.052
ISSN:: 0040-4039

Language:: English
Pubs id:: pubs:40541
UUID:: uuid:607b3406-4258-440e-b313-60da9dc4e620
Local pid:: pubs:40541
Source identifiers:: 40541
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_607b34064258440eb31360da9dc4e620

Terms of use

Copyright date:: 2007

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

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