C2-Oxyanion Neighboring Group Participation: Transition State Structure for the Hydroxide-Promoted Hydrolysis of 4-Nitrophenyl α-d-Mannopyranoside
2016
Speciale, Gaetano | Farren-Dai, Marco | Shidmoossavee, Fahimeh S. | Williams, Spencer J. | Bennet, Andrew J.
The hydroxide-catalyzed hydrolysis of aryl 1,2-trans-glycosides proceeds through a mechanism involving neighboring group participation by a C2-oxyanion and rate-limiting formation of a 1,2-anhydro sugar (oxirane) intermediate. The transition state for the hydroxide-catalyzed hydrolysis of 4-nitrophenyl α-d-mannopyranoside in aqueous media has been studied by the use of multiple kinetic isotope effect (KIE) measurements in conjunction with ab initio theoretical methods. The experimental KIEs are C1-²H (1.112 ± 0.004), C2-²H (1.045 ± 0.005), anomeric 1-¹³C (1.026 ± 0.006), C2-¹³C (0.999 ± 0.005), leaving group oxygen 2-¹⁸O (1.040 ± 0.012), and C2-¹⁸O (1.044 ± 0.006). The transition state for the hydrolysis reaction was modeled computationally using the experimental KIE values as constraints. Taken together, the reported kinetic isotope effects and computational modeling are consistent with the reaction mechanism involving rate-limiting formation of a transient oxirane intermediate that opens in water to give α-d-mannopyranose. The transition state has significant nucleophilic participation by the C2-alkoxide, an essentially cleaved glycosidic bond, and a slight shortening of the endocyclic C1–O5 bond. The TS is late, consistent with the large, normal C2-¹⁸O isotope effect.
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