Journal article

THE ENZYMATIC RING EXPANSION OF PENICILLINS TO CEPHALOSPORINS - SIDE-CHAIN SPECIFICITY

Abstract:: Structural variants of the acylamino side chain of penicillins have been tested as substrates for Deacetoxy/Deacetyl Cephalosporin C Synthetase from C.acremonium CO 728. A six carbon chain terminating in a carboxyl group was found to permit efficient ring expansion to cephems, with the exception of δ-(L-α-aminoadipoyl).1. © 1987.

Publication status:: Published

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APA Style

Baldwin, J., Adlington, R., Crabbe, M., Knight, G., Nomoto, T., Schofield, C., & Ting, H. (1987). THE ENZYMATIC RING EXPANSION OF PENICILLINS TO CEPHALOSPORINS - SIDE-CHAIN SPECIFICITY. TETRAHEDRON, 43(13), 3009–3014.

MLA Style

Baldwin, J., et al. “THE ENZYMATIC RING EXPANSION OF PENICILLINS TO CEPHALOSPORINS - SIDE-CHAIN SPECIFICITY.” TETRAHEDRON, vol. 43, no. 13, 1987, pp. 3009–14.

Chicago Style

Baldwin, J, R Adlington, M Crabbe, G Knight, T Nomoto, C Schofield, and H Ting. 1987. “THE ENZYMATIC RING EXPANSION OF PENICILLINS TO CEPHALOSPORINS - SIDE-CHAIN SPECIFICITY.” TETRAHEDRON 43 (13): 3009–14.
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Publisher copy:: 10.1016/S0040-4020(01)86840-X

Authors

+ Baldwin, J More by this author

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+ Adlington, R More by this author

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+ Crabbe, M More by this author

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+ Knight, G More by this author

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+ Nomoto, T More by this author

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Journal:: TETRAHEDRON More from this journal
Volume:: 43
Issue:: 13
Pages:: 3009-3014
Publication date:: 1987-01-01
DOI:: 10.1016/S0040-4020(01)86840-X
ISSN:: 0040-4020

Language:: English
Pubs id:: pubs:185084
UUID:: uuid:6ed359ed-4fde-485a-8923-b7f8f158c8a0
Local pid:: pubs:185084
Source identifiers:: 185084
Deposit date:: 2012-12-19

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Copyright date:: 1987

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

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