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A Brønsted graph with a convex break at pKa (Lg) = 12.58 provides compelling evidence for an intermediate in the alkaline cyclisation of uridine 3′-phosphate esters. The transient pentacoordinated oxyphosphorane dianion intermediate collapses to reactant and cyclic uridine 2′,3′-monophosphate faster than it can pseudo-rotate and isomerise to the 2′-isomer.

Graphical abstract: Compelling evidence for a stepwise mechanism of the alkaline cyclisation of uridine 3′-phosphate esters

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