Y. Ishibashi, M. Kitamura
Nov 10, 2009
Citations
0
Influential Citations
7
Citations
Journal
Chemical communications
Abstract
By establishing both a highly efficient phosphonamidate formation and a RuCp-catalyzed cleavage of an allyl linker, the solid-phase synthesis of Fmoc-(GlyP(OBn))(6)-OH/DIEA, a protected form of a new type of unnatural peptide alpha-amino phosphonic acid oligomer (APO), has been realized.