Journal article

AMINO-ACID SYNTHESIS VIA RING-OPENING OF N-SULFONYL AZIRIDINE-2-CARBOXYLATE ESTERS WITH ORGANOMETALLIC REAGENTS

Abstract:: Nucleophilic ring opening of optically active N-sulphonyl aziridine-2-carboxylate esters with organometallic reagents has been investigated as a method of preparation of optically active amino acids. © 1993.

Publication status:: Published

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APA Style

Baldwin, J., Spivey, A., Schofield, C., & Sweeney, J. (1993). AMINO-ACID SYNTHESIS VIA RING-OPENING OF N-SULFONYL AZIRIDINE-2-CARBOXYLATE ESTERS WITH ORGANOMETALLIC REAGENTS. TETRAHEDRON, 49(28), 6309–6330.

MLA Style

Baldwin, J, et al. “AMINO-ACID SYNTHESIS VIA RING-OPENING OF N-SULFONYL AZIRIDINE-2-CARBOXYLATE ESTERS WITH ORGANOMETALLIC REAGENTS.” TETRAHEDRON, vol. 49, no. 28, 1993, pp. 6309–30.

Chicago Style

Baldwin, J, A Spivey, C Schofield, and J Sweeney. 1993. “AMINO-ACID SYNTHESIS VIA RING-OPENING OF N-SULFONYL AZIRIDINE-2-CARBOXYLATE ESTERS WITH ORGANOMETALLIC REAGENTS.” TETRAHEDRON 49 (28): 6309–30.
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Publisher copy:: 10.1016/S0040-4020(01)87968-0

Authors

+ Baldwin, J More by this author

Role:: Author

+ Spivey, A More by this author

Role:: Author

+ Schofield, C More by this author

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

+ Sweeney, J More by this author

Role:: Author

Journal:: TETRAHEDRON More from this journal
Volume:: 49
Issue:: 28
Pages:: 6309-6330
Publication date:: 1993-07-09
DOI:: 10.1016/S0040-4020(01)87968-0
ISSN:: 0040-4020

Pubs id:: pubs:44191
UUID:: uuid:d39e5821-febc-4009-ba37-ce645c051f8b
Local pid:: pubs:44191
Source identifiers:: 44191
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_d39e5821febc4009ba37ce645c051f8b

Terms of use

Copyright date:: 1993

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

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