Results 201 to 210 of about 48,198 (269)

Unlocking the Silent Proteome: Chemoselective Asn/Gln Activation for Multidimensional Protein Diversification. [PDF]

J Am Chem Soc
Emenike B, Paikin ZE, Talbott JM, Lidskog A, Gia Le BQ, Swaminathan J, Anslyn EV, Raj M.   +7 more
europepmc   +1 more source

Biochemical and Genetic Characterization of Ergot Alkaloid Biosynthesis in <i>Aspergillus aspearensis</i>. [PDF]

Toxins (Basel)
Fuss JL, Panaccione DG.
europepmc   +1 more source

THE AMIDE NITROGEN OF BLOOD

Journal of Biological Chemistry, 1928
openaire   +2 more sources

Accurate Measurements of Solvent Exchange in Asparagine and Glutamine Side-Chain NH₂ Groups of Proteins by <i>z</i>-Exchange NMR Spectroscopy. [PDF]

J Phys Chem Lett
Tugarinov V, Clore GM.
europepmc   +1 more source

Phosphine-Catalyzed Regio- and Stereoselective Umpolung Addition of Amides to Alkynoates: Access to Complex α,β-Dehydroamino Acid Derivatives. [PDF]

Org Lett
Buchbinder NW, Dunnavant KL, Bage AD, Beck ON, Harris KR, Gwinn RK, Santos WL.   +6 more
europepmc   +1 more source

Development of a Brain-Penetrant Nurr1 Agonist Tool. [PDF]

ChemMedChem
Vietor J, Stiller T, Gege C, Saeb W, López-García Ú, Kohlhof H, Vitt D, Merk D.   +7 more
europepmc   +1 more source

Efficient Synthesis of Amides through Thioacids Reactions with In Situ Generated Formamidine. [PDF]

J Org Chem
Kuo CL, Chen YJ, Chen HJ, Yu CC, Liang CF.   +4 more
europepmc   +1 more source

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Amide–Amide Hydrogen Bonding. Semirubin Amides

Monatshefte für Chemie - Chemical Monthly, 2006
Semirubins are analogs for one-half of the bilirubin structure and capable of intramolecular hydrogen bonding. Semirubin amides of ammonia and primary amines are also capable of intramolecular hydrogen bonding. From a combination of spectroscopic methods (1H NMR, NOE, and VPO), the primary amide is found to engage very effectively in intramolecular ...
Nicholas T. Salzameda, David A. Lightner
openaire   +1 more source

Reactions of amide anions with α-bromo-amides

J. Chem. Soc., Chem. Commun., 1981
The reactions of α-bromoisobutyramides with the anions from amides and a thioamide afford oxazolidin-4-ones and a thiazolidin-4-one, respectively; these are useful intermediates for preparation of ester derivatives.
G. Cavicchioni, SCRIMIN, PAOLO MARIA, A. C. Veronese, F. D'Angeli   +3 more
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Peptide amidation

Trends in Biochemical Sciences, 1991
Many hormones, neurotransmitters and growth factors are peptides that carry an amide group at their carboxyl terminus which is essential for their biological activity. The amide is formed by hydroxylation of an additional glycine residue present in the biosynthetic precursor and the hydroxyglycine derivative dissociates to form the peptide amide and ...
A F, Bradbury, D G, Smyth
openaire   +2 more sources