Journal article

Syntheses of (6S,7S)- and (6S,7R)-deacetoxycephalosporanic acids from 6-aminopenicillanic acid

Abstract:: Two practical (i.e. applicable to multigram scale synthesis) approaches to (6S,7S)-cephalosporins (i.e. the enantiomers of naturally occuring cephalosporins) and the (6S)-epimers of cephalosporins from readily available (2S,5R,6R)-6-aminopenicillanic acid 1 are described.

Publication status:: Published

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APA Style

Fekner, T., Baldwin, J., Adlington, R., & Schofield, C. (1996). Syntheses of (6S,7S)- and (6S,7R)-deacetoxycephalosporanic acids from 6-aminopenicillanic acid. CHEMICAL COMMUNICATIONS, 16, 1989–1990.

MLA Style

Fekner, T, et al. “Syntheses of (6S,7S)- and (6S,7R)-Deacetoxycephalosporanic Acids from 6-Aminopenicillanic Acid.” CHEMICAL COMMUNICATIONS, no. 16, 1996, pp. 1989–90.

Chicago Style

Fekner, T, J Baldwin, R Adlington, and C Schofield. 1996. “Syntheses of (6S,7S)- and (6S,7R)-Deacetoxycephalosporanic Acids from 6-Aminopenicillanic Acid.” CHEMICAL COMMUNICATIONS, no. 16: 1989–90.
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Publisher copy:: 10.1039/cc9960001989

Authors

+ Fekner, T More by this author

Role:: Author

+ Baldwin, J More by this author

Role:: Author

+ Adlington, R 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

Journal:: CHEMICAL COMMUNICATIONS More from this journal
Issue:: 16
Pages:: 1989-1990
Publication date:: 1996-08-21
DOI:: 10.1039/cc9960001989
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Pubs id:: pubs:45330
UUID:: uuid:f4ca27d6-16af-4285-9ab1-fac6522e2363
Local pid:: pubs:45330
Source identifiers:: 45330
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_f4ca27d616af42859ab1fac6522e2363

Terms of use

Copyright date:: 1996

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

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