A general protocol for the synthesis of N-alkyl indoles has been developed via a redox neutral C–H activation strategy using a traceless nitroso directing group. A broad scope of substituted N-alkyl indoles has been prepared in good to excellent yields using a very simple Rh catalyst system in the absence of an external oxidant or any other additive. Good to excellent regioselectivity has been achieved for asymmetrically disubstituted acetylenes
An efficient catalytic cyclization of \u3b2-nitrostyrenes to indoles was developed. The reaction was...
The thermal reaction between nitrosoarenes and alkynes under alkylating conditions produces N-alkoxy...
An efficient route to 2,3-disubstituted indoles was developed via reductive alkylation of 2-substitu...
A general protocol for the synthesis of N-alkyl indoles has been developed via a redox neutral C-H a...
A new strategy is reported for the economical synthesis of indoles bearing an <i>N</i>-(3-aminobut-2...
The redox-neutral annulation of alkynes by differently decorated nitrones set the stage for a step-e...
A distinct C–H activation-based traceless synthetic protocol via electrophilic removal of a directin...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
Unprotected indoles are prepared with the title method, which has a wide scope for alkynes. Excellen...
Rh-catalyzed redox-neutral coupling between N-aryl nitrones and alkynes has been achieved under rela...
An Efficient Route to 2,3-Disubstituted Indoles via Reductive Alkylation Using H2 as Reductan
The first Ru-catalyzed redox-neutral C–H activation reaction via N–N bond cleavage is reported. Pyra...
Versatile nickel catalysts enabled the step-economical synthesis of decorated indoles through alkyne...
The first Ru-catalyzed redox-neutral C-H activation reaction via N-N bond cleavage is reported. Pyra...
The direct CH annulation of anilines or related compounds with internal alkynes provides straightfor...
An efficient catalytic cyclization of \u3b2-nitrostyrenes to indoles was developed. The reaction was...
The thermal reaction between nitrosoarenes and alkynes under alkylating conditions produces N-alkoxy...
An efficient route to 2,3-disubstituted indoles was developed via reductive alkylation of 2-substitu...
A general protocol for the synthesis of N-alkyl indoles has been developed via a redox neutral C-H a...
A new strategy is reported for the economical synthesis of indoles bearing an <i>N</i>-(3-aminobut-2...
The redox-neutral annulation of alkynes by differently decorated nitrones set the stage for a step-e...
A distinct C–H activation-based traceless synthetic protocol via electrophilic removal of a directin...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
Unprotected indoles are prepared with the title method, which has a wide scope for alkynes. Excellen...
Rh-catalyzed redox-neutral coupling between N-aryl nitrones and alkynes has been achieved under rela...
An Efficient Route to 2,3-Disubstituted Indoles via Reductive Alkylation Using H2 as Reductan
The first Ru-catalyzed redox-neutral C–H activation reaction via N–N bond cleavage is reported. Pyra...
Versatile nickel catalysts enabled the step-economical synthesis of decorated indoles through alkyne...
The first Ru-catalyzed redox-neutral C-H activation reaction via N-N bond cleavage is reported. Pyra...
The direct CH annulation of anilines or related compounds with internal alkynes provides straightfor...
An efficient catalytic cyclization of \u3b2-nitrostyrenes to indoles was developed. The reaction was...
The thermal reaction between nitrosoarenes and alkynes under alkylating conditions produces N-alkoxy...
An efficient route to 2,3-disubstituted indoles was developed via reductive alkylation of 2-substitu...