Recommanded Product: Ethyl (2S)-2-amino-3,3-dimethylbutanoateOn November 6, 2020 ,《Peptide modification via N-terminal-residue-directed γ-C(sp3)-H arylation》 appeared in Organic Letters. The author of the article were Hou, Zhen-Lin; Yuan, Feipeng; Yao, Bo. The article conveys some information:
Post-assembly modification of peptides via C(sp3)-H functionalization provides an efficient way to prepare functionalized peptides for biol. study and pharmaceutical development. In this work, we developed a new method for γ-C(sp3)-H functionalization of aliphatic side chains of N-terminus-unprotected peptides. With the N-terminal residues as directing groups, a wide range of di-, tri-, tetra-, and pentapeptides underwent C-H arylation of the residues (Val, Ile, Tle) at the +2 position from the N-terminus. The experimental process involved the reaction of Ethyl (2S)-2-amino-3,3-dimethylbutanoate(cas: 69557-34-2Recommanded Product: Ethyl (2S)-2-amino-3,3-dimethylbutanoate)
Ethyl (2S)-2-amino-3,3-dimethylbutanoate(cas: 69557-34-2) belongs to esters. They are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils.Recommanded Product: Ethyl (2S)-2-amino-3,3-dimethylbutanoate They perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics