Journal article

THE RING EXPANSION OF PENAMS TO CEPHAMS - A POSSIBLE BIOMIMETIC PROCESS

Abstract:: Reaction of a 2β-bromomethyl penam with triphenyltin hydride gave, via ring expansion of the derived 2β-methyl radical, the corresponding cepham system; a similar process may be in operation during the biosynthetic ring expansion of penicillin N to deacetoxycephalasporin C.1. © 1988.

Publication status:: Published

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APA Style

Baldwin, J., Adlington, R., Kang, T., Lee, E., & Schofield, C. (1988). THE RING EXPANSION OF PENAMS TO CEPHAMS - A POSSIBLE BIOMIMETIC PROCESS. TETRAHEDRON, 44(18), 5953–5957.

MLA Style

Baldwin, J, et al. “THE RING EXPANSION OF PENAMS TO CEPHAMS - A POSSIBLE BIOMIMETIC PROCESS.” TETRAHEDRON, vol. 44, no. 18, 1988, pp. 5953–57.

Chicago Style

Baldwin, J, R Adlington, T Kang, E Lee, and C Schofield. 1988. “THE RING EXPANSION OF PENAMS TO CEPHAMS - A POSSIBLE BIOMIMETIC PROCESS.” TETRAHEDRON 44 (18): 5953–57.
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Publisher copy:: 10.1016/S0040-4020(01)81453-8

Authors

+ Baldwin, J More by this author

Role:: Author

+ Adlington, R More by this author

Role:: Author

+ Kang, T More by this author

Role:: Author

+ Lee, E More by this author

Role:: Author

+ Schofield, C More by this author

Role:: Author

Journal:: TETRAHEDRON More from this journal
Volume:: 44
Issue:: 18
Pages:: 5953-5957
Publication date:: 1988-01-01
DOI:: 10.1016/S0040-4020(01)81453-8
ISSN:: 0040-4020

Language:: English
Pubs id:: pubs:42986
UUID:: uuid:1ba8f00c-d986-4cc6-9d5b-294449b911fd
Local pid:: pubs:42986
Source identifiers:: 42986
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_1ba8f00cd9864cc69d5b294449b911fd

Terms of use

Copyright date:: 1988

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

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