Issue 17, 1969

Peptides. Part XXIX. Synthesis of canine gastrin and a new synthesis of human gastrin

Abstract

The heptadecapeptide amide [graphic omitted]lu-Gly-Pro-Trp-Met-Glu-Glu-Ala-Glu-Glu-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH2(canine gastrin I) has been synthesised by a new general route, and the [Leu5,Glu8]-analogue (human gastrin I) by a variant of it. O-Acylation of tyrosine derivatives by N-hydroxysuccinimide esters was found to occur in aqueous but not in anhydrous solution.

Article information

Article type
Paper

J. Chem. Soc. C, 1969, 2213-2217

Peptides. Part XXIX. Synthesis of canine gastrin and a new synthesis of human gastrin

K. L. Agarwal, G. W. Kenner and R. C. Sheppard, J. Chem. Soc. C, 1969, 2213 DOI: 10.1039/J39690002213

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