Mechanism of Permanganate-Promoted Dihydroxylation of Complex Diketopiperazines: Critical Roles of Counter-cation and Ion-Pairing

The mechanism of permanganate-mediated dual C–H oxidation of complex diketo­piperazines has been examined with density functional theory computations. The products of these oxidations are enabling intermediates in the synthesis of structurally diverse ETP natural products. We evaluated, for the first time, the impact of ion-pairing and aggregation states of the permanganate ion and counter-cations, such as bis­(pyridine)-silver­(I) (Ag+) and tetra-n-butyl­ammonium (TBA+), on the C–H oxidation mechanism. The C–H abstraction occurs through an open shell singlet species, as noted previously, followed by O-rebound and a competing OH-rebound pathway. The second C–H oxidation proceeds with a second equivalent of oxidant with lower free energy barriers than the first C–H oxidation due to directing effects and the generation of a more reactive oxidant species after the first C–H oxidation. The success and efficiency of the second C−H oxidation are found to be critically dependent on the presence of an ion-paired oxidant. We used the developed mechanistic knowledge to rationalize an experimentally observed oxidation pattern for C3-indole-substituted diketo­piperazine (+)-5 under optimal oxidation conditions: namely, the formation of diol (−)-6 as a single diastereomer and lack of the ketone products. We proposed two factors that may impede the ketone formation: (i) the conformational flexibility of the diketo­piperazine ring, and (ii) hindrance of this site, making it less accessible to the ion-paired oxidant species.