1, 4-Disubstituted 1, 2, 3-triazoles as amide bond surrogates for the stabilisation of linear peptides with biological activity

LM Rečnik, W Kandioller, TL Mindt - Molecules, 2020 - mdpi.com
Peptides represent an important class of biologically active molecules with high potential for
the development of diagnostic and therapeutic agents due to their structural diversity …

1, 2, 3-Triazoles as amide-bond surrogates in peptidomimetics

IE Valverde, TL Mindt - Chimia, 2013 - chimia.ch
Triazoles represent a class of heterocycles with interesting properties for application in
peptide sciences since they closely resemble amide bonds while being stable to enzymatic …

1, 2, 3-Triazoles as peptide bond isosteres: synthesis and biological evaluation of cyclotetrapeptide mimics

VD Bock, D Speijer, H Hiemstra… - Organic & biomolecular …, 2007 - pubs.rsc.org
Since the discovery of CuI-catalysed click chemistry, the field of peptidomimetics has
expanded to include 1, 4-connected 1, 2, 3-triazoles as useful peptide bond isosteres. Here …

[PDF][PDF] Triazole-based P, N ligands: discovery of an enantioselective copper-catalyzed propargylic amination reaction

RJ Detz - Angew. Chem. Int. Ed, 2008 - dare.uva.nl
A proper copper catalyst with a chiral pyridine-2, 6-bisoxazoline (pybox) ligand was used to
convert a variety of propargylic acetates with different side chains (R= Ar, Bn, Alkyl) into their …

Enantioselective, stereodivergent hydroazidation and hydroamination of allenes catalyzed by acyclic diaminocarbene (ADC) gold (I) complexes

DA Khrakovsky, C Tao, MW Johnson… - Angewandte …, 2016 - Wiley Online Library
The gold‐catalyzed enantioselective hydroazidation and hydroamination reactions of
allenes are presented herein. ADC gold (I) catalysts derived from BINAM were critical for …

Enantioselective Copper‐Catalysed Propargylic Substitution: Synthetic Scope Study and Application in Formal Total Syntheses of (+)‐Anisomycin and (−)‐Cytoxazone

RJ Detz, Z Abiri, R le Griel, H Hiemstra… - … A European Journal, 2011 - Wiley Online Library
A copper catalyst with a chiral pyridine‐2, 6‐bisoxazoline (pybox) ligand was used to
convert a variety of propargylic esters with different side chains (R= Ar, Bn, alkyl) into their …

A convenient scalable one-pot conversion of esters and Weinreb amides to terminal alkynes

HD Dickson, SC Smith, KW Hinkle - Tetrahedron letters, 2004 - Elsevier
Esters and amides undergo reduction to the corresponding aldehydes using DIBAL-H
followed by same pot conversion to terminal alkynes utilizing the Bestmann–Ohira reagent …

Synthesis and reactivity of N‐protected‐α‐amino aldehydes

D Gryko, J Chałko, J Jurczak - Chirality, 2003 - Wiley Online Library
During the last decade α‐amino aldehydes have attracted widespread attention as the
important natural source of chiral substrates useful in stereocontrolled organic synthesis …

Biocatalysis and biotransformation in Brazil: an overview

WG Birolli, IM Ferreira, N Alvarenga, DA Santos… - Biotechnology …, 2015 - Elsevier
This review presents the recent research in biocatalysis and biotransformation in Brazil.
Several substrates were biotransformed by fungi, bacteria and plants. Biocatalytic …

Enzymatic macrocyclization of 1, 2, 3‐triazole peptide mimetics

E Oueis, M Jaspars, NJ Westwood… - Angewandte …, 2016 - Wiley Online Library
The macrocyclization of linear peptides is very often accompanied by significant
improvements in their stability and biological activity. Many strategies are available for their …