A Convenient Synthetic Approach to New α-(9-Fluorenylmethoxycarbonylamino) alkylphosphonic Acid Derivatives

Abstract
Benzyl hydrogen α-(9-fluorenylmethoxycarbonylamino)alkylphosphonates 4, obtained by the sodium metaperiodate oxidation of the corresponding phosphinates 3, were converted to the chloridates 5 and coupled with the N ε-protected lysine benzyl ester to afford peptides 6 containing a phosphonamide bond.

This publication has 0 references indexed in Scilit: