[HTML][HTML] Accelerating chemoselective peptide bond formation using bis (2-selenylethyl) amido peptide selenoester surrogates

L Raibaut, M Cargoët, N Ollivier, YM Chang… - Chemical …, 2016 - pubs.rsc.org
Given the potential of peptide selenoesters for protein total synthesis and the paucity of
methods for the synthesis of these sensitive peptide derivatives, we sought to explore the …

[引用][C] Accelerating chemoselective peptide bond formation using bis (2-selenylethyl) amido peptide selenoester surrogates

M Cargoët, L Raibaut, N Ollivier, Y Min, H Drobecq… - Chemical …, 2016 - hal.science
Accelerating chemoselective peptide bond formation using bis(2-selenylethyl)amido peptide
selenoester surrogates - Archive ouverte HAL Accéder directement au contenu Documentation …

Accelerating chemoselective peptide bond formation using bis (2-selenylethyl) amido peptide selenoester surrogates.

L Raibaut, M Cargoët, N Ollivier, YM Chang… - Chemical …, 2016 - europepmc.org
Given the potential of peptide selenoesters for protein total synthesis and the paucity of
methods for the synthesis of these sensitive peptide derivatives, we sought to explore the …

[PDF][PDF] Accelerating chemoselective peptide bond formation using bis (2-selenylethyl) amido peptide selenoester surrogates

L Raibaut, M Cargoët, N Ollivier, YM Chang… - proteins - pdfs.semanticscholar.org
Given the potential of peptide selenoesters for protein total synthesis and the paucity of
methods for the synthesis of these sensitive peptide derivatives, we sought to explore the …

[HTML][HTML] Accelerating chemoselective peptide bond formation using bis (2-selenylethyl) amido peptide selenoester surrogates

L Raibaut, M Cargoët, N Ollivier, YM Chang… - Chemical …, 2016 - ncbi.nlm.nih.gov
Given the potential of peptide selenoesters for protein total synthesis and the paucity of
methods for the synthesis of these sensitive peptide derivatives, we sought to explore the …

Accelerating chemoselective peptide bond formation using bis (2-selenylethyl) amido peptide selenoester surrogates

L Raibaut, M Cargoët, N Ollivier, YM Chang… - Chemical Science, 2016 - Elsevier
Given the potential of peptide selenoesters for protein total synthesis and the paucity of
methods for the synthesis of these sensitive peptide derivatives, we sought to explore the …

Accelerating chemoselective peptide bond formation using bis (2-selenylethyl) amido peptide selenoester surrogates

L Raibaut, M Cargoët, N Ollivier… - Chemical …, 2016 - pubmed.ncbi.nlm.nih.gov
Given the potential of peptide selenoesters for protein total synthesis and the paucity of
methods for the synthesis of these sensitive peptide derivatives, we sought to explore the …

[引用][C] Accelerating chemoselective peptide bond formation using bis (2-selenylethyl) amido peptide selenoester surrogates

L Raibaut, M Cargoët, N Ollivier, YM Chang… - Chemical …, 2016 - cir.nii.ac.jp
Accelerating chemoselective peptide bond formation using bis(2-selenylethyl)amido peptide
selenoester surrogates | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] …

[引用][C] Accelerating chemoselective peptide bond formation using bis (2-selenylethyl) amido peptide selenoester surrogates

M Cargoët, L Raibaut, N Ollivier, Y Min, H Drobecq… - 2016 - lilloa.univ-lille.fr
Accelerating chemoselective peptide bond formation using bis(2-selenylethyl)amido peptide
selenoester surrogates Toggle navigation English français Aide | Contact | À Propos | Ouvrir …

Accelerating chemoselective peptide bond formation using bis (2-selenylethyl) amido peptide selenoester surrogates

L Raibaut, M Cargoët, N Ollivier, YM Chang… - Chemical …, 2016 - orbi.uliege.be
Given the potential of peptide selenoesters for protein total synthesis and the paucity of
methods for the synthesis of these sensitive peptide derivatives, we sought to explore the …