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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… Expand
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… Expand
2018
2018
Just Add Luminol to Turn the Spotlight on Radziszewski Amidation
Radziszewski amidation, namely the peroxide-mediated conversion of nitriles into amides, is a chemiluminescent reaction involving… Expand
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… Expand
Highly Cited
2017
Highly Cited
2017
Diverse ortho-C(sp2)-H Functionalization of Benzaldehydes Using Transient Directing Groups.
Pd-catalyzed C-H functionalizations promoted by transient directing groups remain largely limited to C-H arylation only. Herein… Expand
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Highly Cited
2012
Highly Cited
2012
Mechanisms of organocatalytic amidation and trans-esterification of aromatic esters as a model for the depolymerization of poly(ethylene) terephthalate.
We describe investigations with B3LYP density functional theory to probe mechanisms for the organocatalyzed depolymerization of… Expand
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