The eliminative deoxofluorination of cyclohexanone derivatives using XtalFluor-E is described. The corresponding monofluoroalkenes are obtained in up to 79% yield. Notably, this one-step procedure occurs at room temperature using readily accessible and cost-effective reagents
The most versatile fluorination reactions for the preparation of up to kg amounts of fluorinated com...
A study focused on the synthesis of a derivative of all-cis phenyl-2,3,5,6-tetrafluorocyclohexane, i...
The palladium-catalyzed defluorinative coupling of 1-aryl-2,2-difluoroalkenes with boronic acids is ...
Metallated haloalkenes were used to open epoxides in moderate to good yield. The homoallylic alcohol...
Metallated haloalkenes were used to open epoxides in moderate to good yield. The homoallylic alcohol...
International audienceHerein we report the hydrodefluorination reaction of trifluoromethylated alken...
XtalFluor-E, [Et2NSF2]BF4, is best known as a useful, versatile and inexpensive commercially availab...
Allyl ethers of trifluoroethanol are transformed to difluorinated analogues of deoxysugars via conci...
Background: 1,1-Difluoroalkenes cannot only be used as valuable precursors for organic synthesis, bu...
Alkenoate 5 prepared on a multigramme scale from trifluoroethanol underwent cycloaddition with furan...
This thesis describes the synthesis of highly substituted geminally difluorinated cyclohexenols base...
The “chlorination/fluorination” technique for aliphatic trifluoromethyl ether synthesis was investig...
A visible-light-promoted redox neutral γ,γ-difluoroallylation of cycloketone oxime ethers with trifl...
Synthesis of several 1,4-disubstituted cyclohexanes, by hydrogenation of sterically hindered and ele...
Direct precursors to analogues of pentopyranoses, 6-deoxyhexoses, and hexoses, in which a CF2 center...
The most versatile fluorination reactions for the preparation of up to kg amounts of fluorinated com...
A study focused on the synthesis of a derivative of all-cis phenyl-2,3,5,6-tetrafluorocyclohexane, i...
The palladium-catalyzed defluorinative coupling of 1-aryl-2,2-difluoroalkenes with boronic acids is ...
Metallated haloalkenes were used to open epoxides in moderate to good yield. The homoallylic alcohol...
Metallated haloalkenes were used to open epoxides in moderate to good yield. The homoallylic alcohol...
International audienceHerein we report the hydrodefluorination reaction of trifluoromethylated alken...
XtalFluor-E, [Et2NSF2]BF4, is best known as a useful, versatile and inexpensive commercially availab...
Allyl ethers of trifluoroethanol are transformed to difluorinated analogues of deoxysugars via conci...
Background: 1,1-Difluoroalkenes cannot only be used as valuable precursors for organic synthesis, bu...
Alkenoate 5 prepared on a multigramme scale from trifluoroethanol underwent cycloaddition with furan...
This thesis describes the synthesis of highly substituted geminally difluorinated cyclohexenols base...
The “chlorination/fluorination” technique for aliphatic trifluoromethyl ether synthesis was investig...
A visible-light-promoted redox neutral γ,γ-difluoroallylation of cycloketone oxime ethers with trifl...
Synthesis of several 1,4-disubstituted cyclohexanes, by hydrogenation of sterically hindered and ele...
Direct precursors to analogues of pentopyranoses, 6-deoxyhexoses, and hexoses, in which a CF2 center...
The most versatile fluorination reactions for the preparation of up to kg amounts of fluorinated com...
A study focused on the synthesis of a derivative of all-cis phenyl-2,3,5,6-tetrafluorocyclohexane, i...
The palladium-catalyzed defluorinative coupling of 1-aryl-2,2-difluoroalkenes with boronic acids is ...
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