Trifluoromethylthiolation-Based Bifunctionalization
of Diazocarbonyl Compounds by Rhodium Catalysis
Version 3 2018-08-17, 08:14
Version 2 2017-08-30, 19:50
Version 1 2017-08-16, 21:09
Posted on 2018-08-17 - 08:14
A new Rh-catalyzed,
three-component reaction for the oxytrifluoromethylthiolation
of α-diazoketones was developed. The SCF3 functionality
was introduced using a stable dibenzenesulfonimide reagent under mild
conditions. Alcohols, acetals, and ethers were used as the alkoxy
sources. Cyclic ethers underwent a trifunctionalization reaction through
the introduction of SCF3, OR, and N(SO2Ph)2 substituents in a single step.
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Lübcke, Marvin; Yuan, Weiming; Szabó, Kálmán J. (2017). Trifluoromethylthiolation-Based Bifunctionalization
of Diazocarbonyl Compounds by Rhodium Catalysis. ACS Publications. Collection. https://doi.org/10.1021/acs.orglett.7b02139
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AUTHORS (3)
ML
Marvin Lübcke
WY
Weiming Yuan
KS
Kálmán J. Szabó
KEYWORDS
α- diazoketones2 substituentsSCF 3 functionalityPhDiazocarbonyl Compoundstrifunctionalization reactionRhodium CatalysisacetalSCF 3oxytrifluoromethylthiolationthree-component reactionTrifluoromethylthiolation-Based BifunctionalizationCyclic ethersdibenzenesulfonimide reagentRh-catalyzedalkoxy sourcesintroduction