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C-terminal peptidyl-valine amidation

The formation of a C-terminal peptidyl-valine amide by hydrolysis and oxidation of an interior Val-Gly peptide in a secreted protein. [RESID:AA0100]
National Institutes of Health

Papers overview

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2019
2019
Enantioselective Synthesis of Yohimbine Analogs by an Organocatalytic and Pot-economic Strategy.
An efficient and one-pot method has been developed for the enantioselective synthesis of pentacyclic indole derivatives with the… 
2018
2018
Cu(I)-Catalyzed amidation/imidation of N-arylglycine ester derivatives via C–N coupling under mild conditions
A mild and efficient reaction protocol for the cross-dehydrogenative carbon–nitrogen (CDCN) coupling of N-arylglycine ester… 
2018
2018
Direct defluorinative amidation-hydrolysis reaction of gem-difluoroalkenes with N,N-dimethylformamide, and primary and secondary amines.
A novel and efficient method for the synthesis of arylacetamides by the reactions of gem-difluoroalkenes with N,N… 
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