Journal article

PENICILLIN BIOSYNTHESIS - DEPENDENCE OF SUBSTRATE STEREOCHEMISTRY ON THE MODE OF 2ND RING-CLOSURE

Abstract:: The stereochemical requirements for the conversion of tripeptides with unsaturated amino acids in the C-terminal position to bicyclic β-lactam products using isopenicillin N synthase was investigated using diastereomeric peptides containing 2R,3S-2-amino-3-methylpent-4-enoic acid and 2R,2R-2-amino-3-methylpent-4-enoic acid.1 1 This work has been published in a preliminary form: J.E. Baldwin, R.M. Adlington, C.J. Schofield, and H.-H Ting, J. Chem. Soc., Chem. Commun., 1989, 758. © 1990.

Publication status:: Published

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APA Style

Baldwin, J., Adlington, R., Schofield, C., & Ting, H. (1990). PENICILLIN BIOSYNTHESIS - DEPENDENCE OF SUBSTRATE STEREOCHEMISTRY ON THE MODE OF 2ND RING-CLOSURE. TETRAHEDRON, 46(17), 6145–6154.

MLA Style

Baldwin, J., et al. “PENICILLIN BIOSYNTHESIS - DEPENDENCE OF SUBSTRATE STEREOCHEMISTRY ON THE MODE OF 2ND RING-CLOSURE.” TETRAHEDRON, vol. 46, no. 17, 1990, pp. 6145–54.

Chicago Style

Baldwin, J, R Adlington, C Schofield, and H Ting. 1990. “PENICILLIN BIOSYNTHESIS - DEPENDENCE OF SUBSTRATE STEREOCHEMISTRY ON THE MODE OF 2ND RING-CLOSURE.” TETRAHEDRON 46 (17): 6145–54.
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Publisher copy:: 10.1016/S0040-4020(01)87936-9

Authors

+ Baldwin, J More by this author

Role:: Author

+ Adlington, R More by this author

Role:: Author

+ Schofield, C More by this author

Role:: Author

+ Ting, H More by this author

Role:: Author

Journal:: TETRAHEDRON More from this journal
Volume:: 46
Issue:: 17
Pages:: 6145-6154
Publication date:: 1990-01-01
DOI:: 10.1016/S0040-4020(01)87936-9
ISSN:: 0040-4020

Language:: English
Pubs id:: pubs:43486
UUID:: uuid:ad3a1f8e-276b-4400-8598-6923601e3f31
Local pid:: pubs:43486
Source identifiers:: 43486
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 1990

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

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