3,3-Difluoro-2-oxindoles can be obtained directly from indoles in moderate yields <i>via</i> electrophilic fluorination using <i>N</i>-fluorobenzenesulfonimide as a mild fluorinating reagent. The presence of <i>tert</i>-butyl hydroperoxide during the reaction, together with additional heating after quenching the reaction with triethylamine, is beneficial to the formation of the desired product
Sulfonyl indoles can be converted into 3-alkylidene-2-oxindoles using NCS as single reagent under fl...
International audienceThe direct dearomative addition of arenes to the C3-position of unprotected in...
A new method for the synthesis of 2-(trifluoromethyl)indoles using easily accessible 2-alkynylanili...
An efficient difluorohydroxylation of substituted indoles leading to 3,3-difluoroindolin-2-ols with ...
A tandem gold(I)-catalyzed aminocylization/fluorination and a two-step, one-pot gold(III)-catalyzed ...
Fluorination of trialkylstannylindoles with caesium fluoroxysulfate or Selectfluor(TM) was investiga...
The use of organometallic reagents for functionalization of arenes and heterocycles has recently bee...
Halogenation of 2-trifluoromethylindole afforded 3-chloro-, 3-bromo- and 3-iodo derivatives in up to...
Many pharmaceuticals have fused ring systems and their bioactivity tends to increase with the introd...
Either two or three C–C bonds are formed in the synthesis of 2-trifluoromethylindoles starting with ...
A novel highly C3 selective metal free trifluoroethylation of indoles using 2,2,2-trifuoroethyl(mesi...
International audienceThis account summarizes our involvement in the development of dearomatization ...
The fluorination of 3-acetyl-2-oxindole with N-fluorobenzenesulfonimide under Lewis acid catalysis u...
The Lautens group has developed many late transition-metal catalyzed protocols for the synthesis of ...
A direct double functionalization involving both difluorination and hydroxylation of enamides is rep...
Sulfonyl indoles can be converted into 3-alkylidene-2-oxindoles using NCS as single reagent under fl...
International audienceThe direct dearomative addition of arenes to the C3-position of unprotected in...
A new method for the synthesis of 2-(trifluoromethyl)indoles using easily accessible 2-alkynylanili...
An efficient difluorohydroxylation of substituted indoles leading to 3,3-difluoroindolin-2-ols with ...
A tandem gold(I)-catalyzed aminocylization/fluorination and a two-step, one-pot gold(III)-catalyzed ...
Fluorination of trialkylstannylindoles with caesium fluoroxysulfate or Selectfluor(TM) was investiga...
The use of organometallic reagents for functionalization of arenes and heterocycles has recently bee...
Halogenation of 2-trifluoromethylindole afforded 3-chloro-, 3-bromo- and 3-iodo derivatives in up to...
Many pharmaceuticals have fused ring systems and their bioactivity tends to increase with the introd...
Either two or three C–C bonds are formed in the synthesis of 2-trifluoromethylindoles starting with ...
A novel highly C3 selective metal free trifluoroethylation of indoles using 2,2,2-trifuoroethyl(mesi...
International audienceThis account summarizes our involvement in the development of dearomatization ...
The fluorination of 3-acetyl-2-oxindole with N-fluorobenzenesulfonimide under Lewis acid catalysis u...
The Lautens group has developed many late transition-metal catalyzed protocols for the synthesis of ...
A direct double functionalization involving both difluorination and hydroxylation of enamides is rep...
Sulfonyl indoles can be converted into 3-alkylidene-2-oxindoles using NCS as single reagent under fl...
International audienceThe direct dearomative addition of arenes to the C3-position of unprotected in...
A new method for the synthesis of 2-(trifluoromethyl)indoles using easily accessible 2-alkynylanili...