111524-96-0Relevant articles and documents
The synthesis of Nα-protected amino hydroxamic acids from Nα-protected amino acids employing versatile chlorinating agent CPI-Cl
Vathsala,Srinivasulu,Santhosh,Sureshbabu, Vommina V.
, p. 449 - 457 (2018)
Racemization free synthesis of Nα-protected amino hydroxamic acids from Nα-protected amino acids employing the versatile chlorinating reagent CPI-Cl has been described in one-pot. The present protocol has shown compability towards urethane protecting groups like Boc, Cbz and Fmoc, and side chain protections of amino acids showed complete tolerance.
HOAt.DCHA as co-coupling agent in the synthesis of peptides employing Fmoc-amino acid chlorides as coupling agents: Application to the synthesis of ss-casomorphin
Sureshbabu, Vommina V.,Chennakrishnareddy, Gundala
experimental part, p. 981 - 988 (2009/12/28)
A simple, efficient and racemization free method for the synthesis of peptides employing Fmoc-amino acid chlorides mediated by HOAtDCHA as a co-coupling agent has been described. This protocol is successfully employed in the synthesis of the pentapeptide H-Pro-Gly-VaI-GIy-VaI-OH (PGVGV), and ss-casomorphin (H-Tyr-Pro-Phe-Pro-Gly-OH) in 85 and 80% yields, respectively.
Synthesis of peptides mediated by potassium salt of 1-hydroxy-7-azabenzotriazole
Gopi, H. N.,Babu, V. V. Suresh
, p. 394 - 396 (2007/10/03)
The potassium salt of 1-hydroxy-7-azabenzotriazole can be used along with acid chlorides of 9-fluorenylmethyloxycarbonylamino acids as coupling agents in peptide bond formation.The acylation reactions are rapid and efficient and can be carried out in an organic medium.The yields as well as purity of the peptides are satisfactory.