Issue 22, 1976

Application of 1,2,4-triazoline-3,5-diones in the synthesis of the piperazic acids (hexahydropyridazine-3-carboxylic acids)

Abstract

Diels–Alder reactions between penta-2,4-dienoic acid (and substituted analogues) and 4-phenyl-1,2,4-triazoline-3,5-dione (or 1,2,4-triazoline-3,5-dione) give adducts which, after hydrogenation and hydrolysis, yield the piperazic acid residues identified in the hydrolysates of the monamycin series of cyclohexadepsipeptide antibiotics.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1976, 2390-2394

Application of 1,2,4-triazoline-3,5-diones in the synthesis of the piperazic acids (hexahydropyridazine-3-carboxylic acids)

C. R. Davies and J. S. Davies, J. Chem. Soc., Perkin Trans. 1, 1976, 2390 DOI: 10.1039/P19760002390

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