Asymmetric Synthesis of ω??Bromo??2 (S)??Methyl Acids as Precursors for Novel Arginine, Lysine, and Mercapto Residues
MK Hadden, KP Kokko, TA Dix
Index: Hadden, M. Kyle; Kokko, Kyle P.; Dix, Thomas A. Synthetic Communications, 2005 , vol. 35, # 12 p. 1675 - 1680
Full Text: HTML
Citation Number: 5
Abstract
Abstract A series of ω??bromo??2 (S)??methyl acids has been synthesized as precursors of novel arginine (Arg), lysine (Lys), and mercapto analogues. These intermediates contain α?? methyl groups and are designed to mask the N??terminal amine when incorporated in pharmaceutically relevant peptides.
Related Articles:
Conjugates of modified cryptophycins and RGD-peptides enter target cells by endocytosis
[Nahrwold, Markus; Weiss, Christine; Bogner, Tobias; Mertink, Felix; Conradi, Jens; Sammet, Benedikt; Palmisano, Ralf; Royo Gracia, Soledad; Preusse, Thomas; Sewald, Norbert Journal of Medicinal Chemistry, 2013 , vol. 56, # 5 p. 1853 - 1864]