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Communication

Chem. Commun., 2009, 6985 - 6987, DOI: 10.1039/b912231a


Solid-phase synthesis of protected -amino phosphonic acid oligomers

Yoshitaka 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.

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