Stereoselective synthesis of the orthogonally protected psudodipeptide H-Tyr(Bzl).psi.[CH2O]Asp(OtBu)-OH was carried out with an intention to use this building block in a construction of isosteric analogues of oostatic tetra- and pentapeptides.
Stereoselective synthesis of the orthogonally protected psudodipeptide H-Tyr(Bzl).psi.[CH2O]Asp(OtBu)-OH was carried out with an intention to use this building block in a construction of isosteric analogues of oostatic tetra- and pentapeptides. (en)