Titlebook: Chemical Protein Synthesis; Xuechen Li Book 2022 The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Scie

ambulance

书目名称Chemical Protein Synthesis影响因子(影响力)




书目名称Chemical Protein Synthesis影响因子(影响力)学科排名




书目名称Chemical Protein Synthesis网络公开度




书目名称Chemical Protein Synthesis网络公开度学科排名




书目名称Chemical Protein Synthesis被引频次




书目名称Chemical Protein Synthesis被引频次学科排名




书目名称Chemical Protein Synthesis年度引用




书目名称Chemical Protein Synthesis年度引用学科排名




书目名称Chemical Protein Synthesis读者反馈




书目名称Chemical Protein Synthesis读者反馈学科排名

Ccu106

Computer Graphics, the Fun, Easy Wayshown to be practically useful under suitable conditions. Herein, we describe the methods of using VyPAL2 for protein macrocyclization and labeling at an Asp residue as well as for protein dual labeling through orthogonal Asp- and Asn-directed ligations. We also describe a method for cell-surface pr

Malfunction

,Improved Handling of Peptide Segments Using Side Chain-Based “Helping Hand” Solubilizing Tools,ng block, Fmoc-Glu(AlHx)-OH, which can be prepared in an efficient process over two purifications. Solubilizing sequences are introduced directly on-resin and later cleaved with palladium-catalyzed transfer under aqueous conditions to restore a native Glu side chain. These two chemical tools are str

恶意

JUST

使痛苦

Total Chemical Synthesis of a SARS-CoV-2 Miniprotein Inhibitor LCB1,tion of traditional solid-phase peptide synthesis. It can achieve high-efficient chemical synthesis of proteins containing more than 300 amino acid residues. Peptide hydrazide, as a valuable reagent equivalent to a thioester peptide, can be easily and efficiently prepared by the Fmoc-based SPPS meth

使痛苦

不怕任性

ANN

Crumple

Ynamide-Mediated Synthetic Approach to Thioamide-Substituted Peptides,proteins by replacing a carbonyl oxygen atom of an amide bond by an sp.-hybridized sulfur atom to precisely introduce a thioamide bond Ψ[CS-NH] into a peptide backbone. The .-thioacyloxyenamide intermediates, originating from ynamide coupling reagent and proteinogenic amino monothioacids, are proved