Results 301 to 310 of about 174,959 (338)
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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
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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
ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
P. D. Bailey +3 more
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AbstractFor Abstract see ChemInform Abstract in Full Text.
P. D. Bailey +3 more
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2022
This chapter discusses enamines. It explains the process of achieving enamine through regaining neutrality by losing a proton adjacent to the iminium moiety. Additionally, these compounds rarely serve as nucleophiles or bases on nitrogen. The chapter discusses the formation of enamines from amine and aldehyde or ketone.
Patrick D. Bailey, Keith M. Morgan
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This chapter discusses enamines. It explains the process of achieving enamine through regaining neutrality by losing a proton adjacent to the iminium moiety. Additionally, these compounds rarely serve as nucleophiles or bases on nitrogen. The chapter discusses the formation of enamines from amine and aldehyde or ketone.
Patrick D. Bailey, Keith M. Morgan
openaire +1 more source
ChemInform, 2006
AbstractFor Abstract see ChemInform Abstract in Full Text.
Y. R. Mahajan, S. M. Weinreb
+4 more sources
AbstractFor Abstract see ChemInform Abstract in Full Text.
Y. R. Mahajan, S. M. Weinreb
+4 more sources
Reactions of amide anions with α-bromo-amides
J. Chem. Soc., Chem. Commun., 1981The 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 +3 more
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Amide-Water and Amide-Amide Hydrogen Bond Strengths
The Journal of Physical Chemistry, 1994David A. Dixon +2 more
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