A reductive amination approach for the synthesis of catalytic peptide foldamers

first crystallographic characterization of an imino surrogate for a peptide bond between two amino acids; -turn conformation stabilized by an intramolecular N-HO=C hydrogen bond; reduction of the imino group allows the formation of the [CH 2 NH] moiety. = vs = vsCurrently being tested.. Reductive amination cappingBifunctional catalytic site Chiral initiator/controller

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Publication Details

Published
2024-09-20
DOI
https://doi.org/10.17952/37eps.2024.p2255
Primary Topic
Chemical Synthesis and Analysis
Type
article
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article

A reductive amination approach for the synthesis of catalytic peptide foldamers

Matteo Pollastrini, Alessandro Moretto
Chemical Synthesis and Analysis
article

A reductive amination approach for the synthesis of catalytic peptide foldamers

Matteo Pollastrini, Alessandro Moretto
article en

Abstract

first crystallographic characterization of an imino surrogate for a peptide bond between two amino acids; -turn conformation stabilized by an intramolecular N-HO=C hydrogen bond; reduction of the imino group allows the formation of the [CH 2 NH] moiety. = vs = vsCurrently being tested.. Reductive amination cappingBifunctional catalytic site Chiral initiator/controller

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A reductive amination approach for the synthesis of catalytic peptide foldamers — Matteo Pollastrini, Alessandro Moretto · (2024) | TGRS Research Map | TGRS