Issue 16, 1988

γ-Lactam formation from tripeptides with isopenicillin N synthase

Abstract

Incubation of isopenicillin N synthase (IPNS) with analogues of the natural substrate [(5S)-5-amino-5-carboxypentanoyl]-L-cysteinyl-D-valine (2) in which the cysteinyl residue was replaced by homocysteine gave epimeric 5-hydroxy γ-lactams (10), with no evidence for the formation of bicyclic products.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 1128-1130

γ-Lactam formation from tripeptides with isopenicillin N synthase

J. E. Baldwin, W. J. Norris, R. T. Freeman, M. Bradley, R. M. Adlington, S. Long-Fox and C. J. Schofield, J. Chem. Soc., Chem. Commun., 1988, 1128 DOI: 10.1039/C39880001128

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements