Issue 0, 1967

Amino-acids and peptides. Part VI. The synthesis, by twinning, of cyclodepsipeptides related to serratamolide

Abstract

A fourteen-membered cyclodepsipeptide has been synthesised by the interaction of two molecules of β-L-leucyloxy-propionyl chloride. A similar synthesis utilising β-(O-t-butyl-DL-seryloxy)propionyl chloride gave two isomers. The relationship of these isomers has been discussed.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 997-1003

Amino-acids and peptides. Part VI. The synthesis, by twinning, of cyclodepsipeptides related to serratamolide

C. H. Hassall, T. G. Martin, J. A. Schofield and J. O. Thomas, J. Chem. Soc. C, 1967, 997 DOI: 10.1039/J39670000997

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