1026388-35-1Relevant academic research and scientific papers
Synthesis of Nα-protected amino acid-derived selenocarbamates employing isocyanates as key intermediates
Sureshbabu, Vommina V.,Naik, Shankar A.
experimental part, p. 2676 - 2685 (2010/11/03)
A simple protocol for the synthesis of Nα-urethane-protected N-alkyl-Se-alkyl selenocarbamate derivatives of amino acids has been described. The reaction of Nα-urethane-protected amino alkyl isocyanates with selenating agent LiAlHSeH and subsequent coupli
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
Facile incorporation of urea pseudopeptides into protease substrate analogue inhibitors
Myers, Adam C.,Kowalski, Jennifer A.,Lipton, Mark A.
, p. 5219 - 5222 (2007/10/03)
A new procedure that employs a one-pot, oxidative Hofmann rearrangement to incorporate a urea linkage into peptide backbones is detailed herein. This methodology was used to replace the scissile peptide bonds of [Leu 5]enkephalin and a hexapept
