Issue 12, 1996

Protection of the indole ring of tryptophan by the nucleophile-stable, acid-cleavable Nin-2,4-dimethylpent-3-yloxycarbonyl (Doc) protecting group

Abstract

The Nin-2,4-dimethylpent-3-yloxycarbonyl (Doc) group is presented as a new protecting group for tryptophan that is stable to nucleophiles and trifluoroacetic acid, suppresses alkylation side reactions and is cleaved by strong acid among with other protecting groups used in Boc solid phase peptide synthesis.

Article information

Article type
Paper

Chem. Commun., 1996, 1471-1472

Protection of the indole ring of tryptophan by the nucleophile-stable, acid-cleavable Nin-2,4-dimethylpent-3-yloxycarbonyl (Doc) protecting group

A. Karlström and A. Undén, Chem. Commun., 1996, 1471 DOI: 10.1039/CC9960001471

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.

Social activity

Spotlight

Advertisements