3392-19-6Relevant articles and documents
Solution-phase synthesis of chiral N-, O-, and S-acyl isopeptides
Liaqat, Sumaira,Panda, Siva S.,Rauf, Abdul,Al-Youbi, Abdulrahman O.,Katritzky, Alan R.
, p. 67 - 72 (2014/01/06)
A convenient synthesis of chiral N-, O-, and S-acyl monoiso- and diisopeptides from di- and tripeptides containing tryptophan, tyrosine, and cysteine units using benzotriazole is reported in solution phase. Georg Thieme Verlag Stuttgart · New York.
A One-Pot Peptide Synthesis via Se-phenyl Carboselenoate in Mixed Aqueous/Organic Solvent System
Ghosh, Sunil Kumar,Singh, Usha,Chandha, Mohindra S.,Mamdapur, Vasant R.
, p. 1566 - 1568 (2007/10/02)
A one pot synthesis of peptides with free C-terminal residues has been accomplished via the active Se-phenyl carboselenoate using diphenyl diselenide, tributylphosphine, and N-methylmorpholine N-oxide in an acetonitrile- water mixed solvent system.Free amino acids and peptides have been used as the amine component without pH adjustment.