Comparison of the rates of alkaline hydrolysis of cyclic phosphonamidates with those of their acyclic analogues, and analysis of the reaction products, indicate that the intermediates or transition states involved in the hydrolysis of the cyclic ester have square-pyramidal, rather than trigonal-bipyramidal geometry.
J. A. Boudreau, C. Brown and R. F. Hudson, J. Chem. Soc., Chem. Commun., 1975, 679 DOI: 10.1039/C39750000679
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