389119-36-2Relevant academic research and scientific papers
Efficient synthesis of O-succinimidyl-(tert-butoxycarbonylamino)methyl carbamates derived from α-amino acids accelerated by ultrasound: Application to the synthesis of ureidodipeptides
Sureshbabu, Vommina V.,Sudarshan, Naremaddepalli S.,Kantharaju
, p. 2168 - 2184 (2008/09/21)
The synthesis of O-succinimidyl-(tert-butoxycarbonylamino)methyl carbamates employing isocyanates made through the Curtius rearrangement of Boc-amino acid azides in the presence of N-hydroxysuccinimide under the influence of ultrasound is described. Copyright Taylor & Francis Group, LLC.
Succinimidyl carbamate derivatives from N-protected α-amino acids and dipeptides-synthesis of ureidopeptides and oligourea/peptide hybrids
Fischer, Lucile,Semetey, Vincent,Lozano, Jose-Manuel,Schaffner, Arnaud-Pierre,Briand, Jean-Paul,Didierjean, Claude,Guichard, Gilles
, p. 2511 - 2525 (2008/03/13)
The preparation of succinimidyl (1-{[(alkyloxy)carbonyl]-amino}-1-X-methyl) carbamates (4) and succinimidyl [1-(acyl-amino)-1-X-methyl] carbamates (5) from a variety of N-Boc-, -Z- or -Fmoc-protected α-amino acids and dipeptides as well as the carbamate s
Unexpected stability of the urea cis-trans isomer in urea-containing model pseudopeptides
Semetey, Vincent,Hemmerlin, Christine,Didierjean, Claude,Schaffner, Arnaud-Pierre,Giner, Ana Gimenez,Aubry, Andre,Briand, Jean-Paul,Marraud, Michel,Guichard, Gilles
, p. 3843 - 3845 (2007/10/03)
Equation Presented In contrast to the situation observed in the crystal state, the urea moiety in N-Boc-N-carbamoyl-gem-diaminoalkyl derivatives (single-residue ureidopeptides) 1-4 exclusively assumes a cis-trans conformation in solution. When R3/su
