Stereoselective syntheses and reactions of stannylated peptides

66Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.
Get full text

Abstract

In one fell swoop: Stannylated allyl carbonates allow the highly stereoselective synthesis of metalated peptides, which can be further modified by Stille coupling. Tin-iodine exchange generates iodinated peptides which also can be used for C-C coupling reactions. Therefore, only one stereoselective reaction is necessary to generate a wide range of different peptides in stereochemically pure form. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.

Cite

CITATION STYLE

APA

Deska, J., & Kazmaier, U. (2007). Stereoselective syntheses and reactions of stannylated peptides. Angewandte Chemie - International Edition, 46(24), 4570–4573. https://doi.org/10.1002/anie.200700759

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free