Manganese-Catalyzed Asymmetric Oxidation of Methylene
C–H of Spirocyclic Oxindoles and Dihydroquinolinones with Hydrogen
Peroxide
Version 2 2019-01-11, 19:53
Version 1 2019-01-11, 19:48
Posted on 2019-01-11 - 19:53
A highly
efficient strategy for the enantioselective oxidation
of methylene C–H of spirocyclic oxindoles and dihydroquinolinones
has been established, in which an earth-abundant manganese catalyst
and hydrogen peroxide are used. Noteworthy, the manganese catalyst
can be applied to the asymmetric hydroxylation of spirocyclic 2,3-dihydroquinolin-4-ones
with 94–99% ee.
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Qiu, Bin; Xu, Daqian; Sun, Qiangsheng; Lin, Jin; Sun, Wei (2019). Manganese-Catalyzed Asymmetric Oxidation of Methylene
C–H of Spirocyclic Oxindoles and Dihydroquinolinones with Hydrogen
Peroxide. ACS Publications. Collection. https://doi.org/10.1021/acs.orglett.8b03652
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AUTHORS (5)
BQ
Bin Qiu
DX
Daqian Xu
QS
Qiangsheng Sun
JL
Jin Lin
WS
Wei Sun
KEYWORDS
eeSpirocyclic OxindolesHydrogen PeroxidemethylenedihydroquinolinstrategyDihydroquinolinoneenantioselective oxidation-4-onemanganese catalysthydrogen peroxideearth-abundant manganese catalystspirocyclic oxindolesdihydroquinolinoneManganese-Catalyzed Asymmetric OxidationNoteworthyhydroxylationMethylene