1026388-35-1Relevant articles and documents
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
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
