Journal
ORGANIC LETTERS
Volume 24, Issue 41, Pages 7611-7616Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c03073
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Funding
- National Key Research and Develop- ment Program of China
- National Natural Science Foundation of China
- Science and Technology Commission of Shanghai Municipality
- [2021YFF0701700]
- [21971252]
- [21991122]
- [22271181]
- [22ZR1423600]
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Here, we report the design and synthesis of a difluoromethylsulfonyl imidazolium salt, which serves as a radical difluoromethylation reagent for achieving amino- and oxy-difluoromethylation of alkenes. Importantly, the synthesis of the imidazolium salt can be accomplished without the need for distillation or column chromatography purification, and the amino- and oxy-difluoromethylation pathways are determined by the choice of reaction solvents.
Herein, we describe the design and synthesis of a difluoromethylsulfonyl imidazolium salt, which can act as a radical difluoromethylation reagent to achieve the challenging amino-and oxy-difluoromethylation of alkenes. Notably, the three steps for the synthesis of the imidazolium salt do not require any tedious distillation or column chromatography purification process, and the amino-and oxy-difluoromethylation paths are simply determined by the selection of reaction solvents.
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