4628-56-2Relevant academic research and scientific papers
Peptide ligation assisted by an auxiliary attached to amidyl nitrogen
Li, Juan,Cui, Hong-Kui,Liu, Lei
scheme or table, p. 1793 - 1796 (2010/06/13)
New thiol-containing auxiliaries were developed for peptide ligation. They were placed at the amidyl N-atom in the second amino acid residue of a peptide fragment. With the new auxiliaries, peptide ligation could be conducted at non-Cys and non-Gly sites. Compared to other recently developed auxiliaries, an important feature of the present design was that the new auxiliaries were generally applicable and readily removable.
Synthesis and Kinetics of the Formation of N-Substituted Cyclic Sulfinamides from Secondary Amine Disulfides
Wagner, Barbara J.,Doi, Joyce Takahashi,Musker, W. Kenneth
, p. 4156 - 4162 (2007/10/02)
N-substituted cyclic saturated sulfinamides were prepared from two secondary amine disulfides, 3-propyl disulfide and 3-(cyclohexylamino)propyl disulfide, and two bicyclic sulfinamides were made from 2-(2-piperidyl)ethyl disulfide an
