Communication
Chem. Commun., 2009, 6985 - 6987, DOI: 10.1039/b912231a
Solid-phase synthesis of protected
-amino phosphonic acid oligomersYoshitaka Ishibashi and Masato Kitamura
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
-amino phosphonic acid oligomer (APO), has been realized.
