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

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書目名稱Chemical Protein Synthesis影響因子(影響力)




書目名稱Chemical Protein Synthesis影響因子(影響力)學(xué)科排名




書目名稱Chemical Protein Synthesis網(wǎng)絡(luò)公開度




書目名稱Chemical Protein Synthesis網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Chemical Protein Synthesis被引頻次




書目名稱Chemical Protein Synthesis被引頻次學(xué)科排名




書目名稱Chemical Protein Synthesis年度引用




書目名稱Chemical Protein Synthesis年度引用學(xué)科排名




書目名稱Chemical Protein Synthesis讀者反饋




書目名稱Chemical Protein Synthesis讀者反饋學(xué)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

惡意

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

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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