Issue 10, 1992

Efficient one-step synthesis of diastereoisomeric cyclic dipeptides from amino acids: three diastereoisomers of cyclo-L-isoleucyl-L-isoleucine

Abstract

Cyclic dipeptides formed by the self-condensation of amino acids in ethane-1,2-diol comprise readily separable diastereoisomeric mixtures which, in the case of isoleucine, affords three isomers in good yield.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1992, 1199-1201

Efficient one-step synthesis of diastereoisomeric cyclic dipeptides from amino acids: three diastereoisomers of cyclo-L-isoleucyl-L-isoleucine

B. Cook, R. R. Hill and G. E. Jeffs, J. Chem. Soc., Perkin Trans. 1, 1992, 1199 DOI: 10.1039/P19920001199

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