864960-95-2Relevant academic research and scientific papers
PhenoFluorMix: Practical chemoselective deoxyfluorination of phenols
Fujimoto, Teppei,Ritter, Tobias
supporting information, p. 544 - 547 (2015/03/05)
A practical deoxyfluorination with novel deoxyfluorinating reagent PhenoFluorMix, a mixture of N,N'-1,3-bis(2,6-diisopropylphenyl)chloroimidazolium chloride and CsF, is presented. PhenoFluorMix overcomes the challenges associated with hydrolysis of PhenoFluor. PhenoFluorMix does not hydrolyze, is readily available on decagram scale, and is storable in air. In this paper, we demonstrate the practicality of the reagent and exhibit the deoxyfluorination of a variety of phenols and heterocycles.
FLUORINATION OF ORGANIC COMPOUNDS
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Page/Page column 25, (2012/11/06)
Methods for fluorinating organic compounds are described herein.
Deoxyfluorination of phenols
Tang, Pingping,Wang, Weike,Ritter, Tobias
supporting information; experimental part, p. 11482 - 11484 (2011/10/02)
An operationally simple ipso fluorination of phenols with a new deoxyfluorination reagent is presented.
Heterocyclic compound having oxime group
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Page/Page column 36, (2010/02/14)
The present invention provides a compound that has an excellent inhibitory activity on STAT6 activation and is effective against allergic diseases, and a medicinal composition thereof. According to the present invention, disclosed is the compound represented by the General Formula (I) [where R1 and R2 independently represent a C1-6 alkyl group and the like that may have a hydrogen atom or a substituent; R3 represents a C1-6 alkyl group and the like that may have a substituent; R4 and R5 independent represents a hydrogen atom or a C1-6 alkyl group and the like that may have a substituent; R6 represents a hydrogen atom and the like; W represents —SO2— and the like; and X represents a sulphur atom and the like.]or a salt thereof, or a hydrate thereof.
