A high yield and rapid synthesis of enantiomerically pure N α -protected amino/peptide acid arylamides using n-propylphosphonic anhydride (T3P) in presence of N-methylmorpholine is described. The generality of the reaction has been studied for various N α -protected amino acids with diverse range of aromatic amines and coumarin derivatives
Abstract: The direct conversion of simple and sterically hindered Nα-protected amino/peptide hydrox...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in ...
A high yield and rapid synthesis of enantiomerically pure N (alpha) -protected amino/peptide acid ar...
Thioacids derived from N-protected amino or dipeptide and tripeptide acids undergo facile N-acylatio...
A general, mild, efficient, and environmentally benign protocol, which makes use of T3P® as an acid ...
One-pot preparation of N α -protected amino/peptide hydroxamic acids from corresponding carboxylic a...
A mild and cost-efficient chemo-enzymatic method for the synthesis of C-terminal arylamides of amino...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
A mild and cost-efficient chemo-enzymatic method for the synthesis of C-terminal arylamides of amino...
The direct conversion of simple and sterically hindered Nα-protected amino/peptide hydroxamic acids ...
A simple and efficient method for the synthesis of alcohols from the corresponding carboxylic acids ...
β-Amino acids X-NHCHRCH2CO2H (X = Z, Boc, or Fmoc protecting group; R = PhCH2, Me2CH, Ph, Me) were...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
Abstract: The direct conversion of simple and sterically hindered Nα-protected amino/peptide hydrox...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in ...
A high yield and rapid synthesis of enantiomerically pure N (alpha) -protected amino/peptide acid ar...
Thioacids derived from N-protected amino or dipeptide and tripeptide acids undergo facile N-acylatio...
A general, mild, efficient, and environmentally benign protocol, which makes use of T3P® as an acid ...
One-pot preparation of N α -protected amino/peptide hydroxamic acids from corresponding carboxylic a...
A mild and cost-efficient chemo-enzymatic method for the synthesis of C-terminal arylamides of amino...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
A mild and cost-efficient chemo-enzymatic method for the synthesis of C-terminal arylamides of amino...
The direct conversion of simple and sterically hindered Nα-protected amino/peptide hydroxamic acids ...
A simple and efficient method for the synthesis of alcohols from the corresponding carboxylic acids ...
β-Amino acids X-NHCHRCH2CO2H (X = Z, Boc, or Fmoc protecting group; R = PhCH2, Me2CH, Ph, Me) were...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
Abstract: The direct conversion of simple and sterically hindered Nα-protected amino/peptide hydrox...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in ...