α, β‐Unsaturated γ‐Peptide Foldamers
B Legrand, LT Maillard - ChemPlusChem, 2021 - Wiley Online Library
Despite their concomitant emergence in the 1990s, γ‐peptide foldamers have not developed
as fast as β‐peptide foldamers and to date, only a few γ‐oligomer structures have been …
as fast as β‐peptide foldamers and to date, only a few γ‐oligomer structures have been …
HBTU Mediated Synthesis of α,β‐Unsaturated γ‐Lactams from E‐α,β‐Unsaturated γ‐Amino Acids
The α, β‐unsaturated γ‐lactams have been found in many biologically active peptide natural
products. Due to their biological activities, extensive efforts have been made in the literature …
products. Due to their biological activities, extensive efforts have been made in the literature …
Non‐classical Helices with cis Carbon–Carbon Double Bonds in the Backbone: Structural Features of α,γ‐Hybrid Peptide Foldamers
M Ganesh Kumar, VJ Thombare… - Angewandte …, 2016 - Wiley Online Library
The impact of geometrically constrained cis α, β‐unsaturated γ‐amino acids on the folding of
α, γ‐hybrid peptides was investigated. Structure analysis in single crystals and in solution …
α, γ‐hybrid peptides was investigated. Structure analysis in single crystals and in solution …
Self-Assembly to Function: Design, Synthesis, and Broad Spectrum Antimicrobial Properties of Short Hybrid E-Vinylogous Lipopeptides
SS Shankar, SN Benke, N Nagendra… - Journal of Medicinal …, 2013 - ACS Publications
Nonribosomal E-vinylogous γ-amino acids are widely present in many peptide natural
products and have been exploited as inhibitors for serine and cysteine proteases. Here, we …
products and have been exploited as inhibitors for serine and cysteine proteases. Here, we …
α/γ 4-Hybrid peptide helices: synthesis, crystal conformations and analogy with the α-helix
A Bandyopadhyay, SV Jadhav, HN Gopi - Chemical Communications, 2012 - pubs.rsc.org
Synthesis, crystal conformations of α/γ4-hybrid peptide helices containing proteinogenic
amino acid side-chains, and the analogy with the α-helix are reported. Results suggest that …
amino acid side-chains, and the analogy with the α-helix are reported. Results suggest that …
Comparison of backbone modification in protein β-sheets by α→ γ residue replacement and α-residue methylation
GA Lengyel, ZE Reinert, BD Griffith… - Organic & biomolecular …, 2014 - pubs.rsc.org
The mimicry of protein tertiary structure by oligomers with unnatural backbones is a
significant contemporary research challenge. Among common elements of secondary …
significant contemporary research challenge. Among common elements of secondary …
Introduction of cyclically constrained γ-residues stabilizes an α-peptide hairpin in aqueous solution
GA Lengyel, GA Eddinger, WS Horne - Organic letters, 2013 - ACS Publications
The synthesis and structural characterization of hybrid α/γ-peptides resulting from a 1: 1 α→
γ residue substitution at cross-strand positions in a hairpin-forming α-peptide sequence are …
γ residue substitution at cross-strand positions in a hairpin-forming α-peptide sequence are …
Hybrid peptides: Direct transformation of α/α, β-unsaturated γ-hybrid peptides to α/γ-hybrid peptide 12-helices
A Bandyopadhyay, HN Gopi - Organic Letters, 2012 - ACS Publications
Hybrid Peptides: Direct Transformation of α/α, β-Unsaturated γ-Hybrid Peptides to α/γ-Hybrid
Peptide 12-Helices | Organic Letters ACS ACS Publications C&EN CAS Find my institution Log …
Peptide 12-Helices | Organic Letters ACS ACS Publications C&EN CAS Find my institution Log …
Exploring β-hydroxy γ-amino acids (statines) in the design of hybrid peptide foldamers
Exploring β-Hydroxy γ-Amino Acids (Statines) in the Design of Hybrid Peptide Foldamers |
Organic Letters ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters …
Organic Letters ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters …
Direct Transformation of N-Protected α, β-Unsaturated γ-Amino Amides into γ-Lactams through a Base-Mediated Molecular Rearrangement
M Ganesh Kumar, K Veeresh… - The Journal of …, 2019 - ACS Publications
Here, we are reporting a single-step transformation of N-protected α, β-unsaturated γ-amino
amides into 5, 5-disubstituted γ-lactams through a base-mediated new molecular …
amides into 5, 5-disubstituted γ-lactams through a base-mediated new molecular …