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Updated: Jun 22, 2026

Split-and-pool Synthesis and Characterization of Peptide Tertiary Amide Library
Published on: June 20, 2014
New tetracyclic tetrahydro-beta-carbolines as tryptophan-derived peptidomimetics
Karolina Pulka1, Debby Feytens, Aleksandra Misicka
1Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093, Warsaw, Poland. karola@chem.uw.edu.pl
Abstract:
The Pictet-Spengler reaction is known as a useful tool for the synthesis of constrained analogs of tryptophan. Herein, we present the further cyclization of 1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid methyl esters with 1-(1'-aminoalkyl) side chain. These transformations lead to heterocyclic structures which can find useful applications in medicinal chemistry as peptide mimetics.
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