The direct coupling of readily available nitroalkane and amines with just S8 and Na2S, provides an efficient way to make thioamides and thiopeptides. Mechanistic insights indicated acyl nitrite was the key intermediates. With this in-situ generated thioacylating reagents, a wide of thioamide-containing bioactive compounds were easily prepared
The synthesis and reactivity of fully protected thioamide analogues of asparagine and glutamine are ...
Ligation reactions have emerged as an important tool for the chemoselective conjugation of large and...
Thioacids derived from N-protected amino or dipeptide and tripeptide acids undergo facile N-acylatio...
The direct coupling of readily available nitroalkane and amines with just S8 and Na2S, provides an e...
1-Amino-1-methylthio-2-nitroethenes (2) can be converted in high yields to the Nitroacetamides (3) b...
New thionation experimental conditions and new reagents for the synthesis of thioamide analogues of ...
Vital roles of peptide/protein thioesters in protein chemistry, including chemical or semi synthesis...
© 2018 Dr. Jing (Katherine) ShangPeptide therapeutics are used directly or as carriers of cytotoxic ...
Peptide thioesters are very useful in protein chemistry, and chemistry- and biochemistry-based proto...
The preparation of N-thioformyl peptides from amino thioacids and isonitriles at room temperature is...
The thiol-ene ‘click’ reaction has emerged as a versatile process for carbon–sulfur bond formation w...
A one-pot procedure for the synthesis of thioesters from primary amines is reported. Polyamides cont...
A simple and efficient method for the synthesis of thiopeptides by the treatment of Nα-protected pep...
© 2016 Dr. Aysa PourvaliThe synthesis of amide bonds is one the most important issues in organic che...
Thioacids derived from N-protected amino or dipeptide and tripeptide acids undergo facile N-acylatio...
The synthesis and reactivity of fully protected thioamide analogues of asparagine and glutamine are ...
Ligation reactions have emerged as an important tool for the chemoselective conjugation of large and...
Thioacids derived from N-protected amino or dipeptide and tripeptide acids undergo facile N-acylatio...
The direct coupling of readily available nitroalkane and amines with just S8 and Na2S, provides an e...
1-Amino-1-methylthio-2-nitroethenes (2) can be converted in high yields to the Nitroacetamides (3) b...
New thionation experimental conditions and new reagents for the synthesis of thioamide analogues of ...
Vital roles of peptide/protein thioesters in protein chemistry, including chemical or semi synthesis...
© 2018 Dr. Jing (Katherine) ShangPeptide therapeutics are used directly or as carriers of cytotoxic ...
Peptide thioesters are very useful in protein chemistry, and chemistry- and biochemistry-based proto...
The preparation of N-thioformyl peptides from amino thioacids and isonitriles at room temperature is...
The thiol-ene ‘click’ reaction has emerged as a versatile process for carbon–sulfur bond formation w...
A one-pot procedure for the synthesis of thioesters from primary amines is reported. Polyamides cont...
A simple and efficient method for the synthesis of thiopeptides by the treatment of Nα-protected pep...
© 2016 Dr. Aysa PourvaliThe synthesis of amide bonds is one the most important issues in organic che...
Thioacids derived from N-protected amino or dipeptide and tripeptide acids undergo facile N-acylatio...
The synthesis and reactivity of fully protected thioamide analogues of asparagine and glutamine are ...
Ligation reactions have emerged as an important tool for the chemoselective conjugation of large and...
Thioacids derived from N-protected amino or dipeptide and tripeptide acids undergo facile N-acylatio...