Versatile nickel catalysts enabled the step-economical synthesis of decorated indoles through alkyne annulations with anilines bearing removable directing groups. The C-H/N-H activation strategy efficiently occurred in the absence of any metal oxidants and with excellent selectivities.peerReviewe
Tandem palladium-catalysed aryl and alkenyl C-N bond formation allows the synthesis of a variety of ...
A general protocol for the synthesis of N-alkyl indoles has been developed via a redox neutral C–H a...
The direct CH annulation of anilines or related compounds with internal alkynes provides straightfor...
A nickel-catalyzed direct C-2 alkylation of indoles through monodentate-chelation assistance has bee...
Efforts toward the development of a regioselective synthesis of functionalized indoles with nickel c...
Nickel-catalyzed regioselective C–H bond alkenylation of indoles and related heteroarenes with alken...
Pd doles it out: A palladium-catalyzed approach to indoles using the title reaction was achieved (se...
The redox-neutral annulation of alkynes by differently decorated nitrones set the stage for a step-e...
A one-pot cascade approach for the synthesis of N-substituted indoles from amino alcohols and alcoho...
The selective N-alkylation of amines with alcohols via the borrowing hydrogen strategy represents a ...
Nickel/photoredox catalysis is used to synthesize indolines in one step from iodoacetanilides and al...
The prevalence of indoles in bioactive molecules1 has prompted the development of many useful method...
International audienceHerein, we demonstrated that 2-alkynyldimethylamines easily cyclize in EtOH ac...
Direct homologation of aromatic amides with internal alkynes has been accomplished via a nickel-cata...
A new regioselective method for the synthesis of multifunctionalized indoles from [3 + 2] annulation...
Tandem palladium-catalysed aryl and alkenyl C-N bond formation allows the synthesis of a variety of ...
A general protocol for the synthesis of N-alkyl indoles has been developed via a redox neutral C–H a...
The direct CH annulation of anilines or related compounds with internal alkynes provides straightfor...
A nickel-catalyzed direct C-2 alkylation of indoles through monodentate-chelation assistance has bee...
Efforts toward the development of a regioselective synthesis of functionalized indoles with nickel c...
Nickel-catalyzed regioselective C–H bond alkenylation of indoles and related heteroarenes with alken...
Pd doles it out: A palladium-catalyzed approach to indoles using the title reaction was achieved (se...
The redox-neutral annulation of alkynes by differently decorated nitrones set the stage for a step-e...
A one-pot cascade approach for the synthesis of N-substituted indoles from amino alcohols and alcoho...
The selective N-alkylation of amines with alcohols via the borrowing hydrogen strategy represents a ...
Nickel/photoredox catalysis is used to synthesize indolines in one step from iodoacetanilides and al...
The prevalence of indoles in bioactive molecules1 has prompted the development of many useful method...
International audienceHerein, we demonstrated that 2-alkynyldimethylamines easily cyclize in EtOH ac...
Direct homologation of aromatic amides with internal alkynes has been accomplished via a nickel-cata...
A new regioselective method for the synthesis of multifunctionalized indoles from [3 + 2] annulation...
Tandem palladium-catalysed aryl and alkenyl C-N bond formation allows the synthesis of a variety of ...
A general protocol for the synthesis of N-alkyl indoles has been developed via a redox neutral C–H a...
The direct CH annulation of anilines or related compounds with internal alkynes provides straightfor...