Journal
ACS CENTRAL SCIENCE
Volume 3, Issue 3, Pages 196-204Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acscentsci.6b00368
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Funding
- MINECO of Spain [CTQ2015-70795-P]
- Catalan DIUE of the Generalitat de Catalunya [2009SGR637]
- ICREA-Academia award
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Monosubstituted cycloalkanes undergo regio- and enantioselective aliphatic C H oxidation with H2O2 catalyzed by biologically inspired manganese catalysts. The reaction furnishes the corresponding ketones resulting from oxidation at C3 and C4 methylenic sites (K-3 and K-4, respectively) leading to a chiral desymmetrization that proceeds with remarkable enantioselectivity (64% ee) but modest regioselectivity at C3 (K-3/K-4 approximate to 2) for tert-butylcyclohexane, and with up to 9696 ee and exquisite regioselectity toward C3 (up to K-3/K-4 > 99) when N-cyclohexylalkanamides are employed as substrates. Efficient H2O2 activation, high yield, and highly enantioselective C H oxidation rely on the synergistic cooperation of a sterically bulky manganese catalyst and an oxidatively robust alkanoic acid. This represents the first example of nonenzymatic highly enantioselective oxidation of nonactivated methylenic sites. Furthermore, the principles of catalyst design disclosed in this work constitute a unique platform for further development of stereoselective C H oxidation reactions.
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