A method for direct, transition-metal-free <i>ortho</i>-arylation of anilines by aryl chlorides, bromides, fluorides, and triflates has been developed. This methodology provides the most direct approach to 2-arylanilines since no protecting or directing groups on nitrogen are required. The arylation is functional-group tolerant, with alkene, ether, trifluoromethyl, dimethylamino, carbonyl, chloro, and cyano functionalities tolerated. Phenylation of enantiopure binaphthyldiamine affords a product with >99% ee
Direct arylations of pyridines are challenging transformations due to the high Lewis basicity of the...
International audienceThe palladium-catalyzed C-C bond formation via direct arylation of free-amine-...
A synthetic methodology for the late-stage ortho-C–H bond aroylation of anilines with aryl aldehydes...
A transition metal-free N-arylation of primary and secondary amines with diaryliodonium salts is pre...
The ortho arylation of anilides to form biphenyls via a twofold C−H functionalization/C−C bond-formi...
A visible-light-mediated, catalyst-free, direct (hetero)arylation of anilines with mild reaction con...
We report the synthesis of fluorinated anilines by palladium-catalyzed coupling of fluoroalkylamines...
The highly monoselective N-arylation of aromatic tertiary amines using a transition-metal-free appro...
Producción CientíficaMetal-catalyzed C–H functionalizations on the aryl ring of anilines usually nee...
A method for base-promoted arylation of arenes and heterocycles by aryl halides and aryl triflates i...
Herein, we disclose the first <i>metal-free</i> synthesis of primary aromatic amines from arylboroni...
Substituted 2-aminobiphenyls have been prepared from arylhydrazine hydrochlorides and anilines in bi...
Palladium-catalyzed <i>ortho</i>-arylation of anilides was achieved using 2-aminophenyl-1<i>H</i>-py...
Anilines are key constituents in biologically active compounds and often obtained from transition me...
A new palladium-catalyzed, heteroatom-directed strategy for C–H nitration of anilines is described. ...
Direct arylations of pyridines are challenging transformations due to the high Lewis basicity of the...
International audienceThe palladium-catalyzed C-C bond formation via direct arylation of free-amine-...
A synthetic methodology for the late-stage ortho-C–H bond aroylation of anilines with aryl aldehydes...
A transition metal-free N-arylation of primary and secondary amines with diaryliodonium salts is pre...
The ortho arylation of anilides to form biphenyls via a twofold C−H functionalization/C−C bond-formi...
A visible-light-mediated, catalyst-free, direct (hetero)arylation of anilines with mild reaction con...
We report the synthesis of fluorinated anilines by palladium-catalyzed coupling of fluoroalkylamines...
The highly monoselective N-arylation of aromatic tertiary amines using a transition-metal-free appro...
Producción CientíficaMetal-catalyzed C–H functionalizations on the aryl ring of anilines usually nee...
A method for base-promoted arylation of arenes and heterocycles by aryl halides and aryl triflates i...
Herein, we disclose the first <i>metal-free</i> synthesis of primary aromatic amines from arylboroni...
Substituted 2-aminobiphenyls have been prepared from arylhydrazine hydrochlorides and anilines in bi...
Palladium-catalyzed <i>ortho</i>-arylation of anilides was achieved using 2-aminophenyl-1<i>H</i>-py...
Anilines are key constituents in biologically active compounds and often obtained from transition me...
A new palladium-catalyzed, heteroatom-directed strategy for C–H nitration of anilines is described. ...
Direct arylations of pyridines are challenging transformations due to the high Lewis basicity of the...
International audienceThe palladium-catalyzed C-C bond formation via direct arylation of free-amine-...
A synthetic methodology for the late-stage ortho-C–H bond aroylation of anilines with aryl aldehydes...