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.http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000326121700038&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701Chemistry, OrganicSCI(E)PubMed104ARTICLE205294-52971
A highly regioselective functionalization of indole at the C-4 position by employing an aldehyde fun...
The first example of Rh(III)-catalyzed cyclization of arylnitrones to indolines under external oxida...
Regioselective direct functionalization of an indole benzenoid fragment has been a significant chall...
A general protocol for the synthesis of N-alkyl indoles has been developed via a redox neutral C–H a...
A distinct C–H activation-based traceless synthetic protocol via electrophilic removal of a directin...
A new strategy is reported for the economical synthesis of indoles bearing an <i>N</i>-(3-aminobut-2...
Unprotected indoles are prepared with the title method, which has a wide scope for alkynes. Excellen...
The redox-neutral annulation of alkynes by differently decorated nitrones set the stage for a step-e...
The first Ru-catalyzed redox-neutral C-H activation reaction via N-N bond cleavage is reported. Pyra...
An Efficient Route to 2,3-Disubstituted Indoles via Reductive Alkylation Using H2 as Reductan
Rh-catalyzed redox-neutral coupling between N-aryl nitrones and alkynes has been achieved under rela...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
Versatile nickel catalysts enabled the step-economical synthesis of decorated indoles through alkyne...
An efficient route to 2,3-disubstituted indoles was developed via reductive alkylation of 2-substitu...
Pd doles it out: A palladium-catalyzed approach to indoles using the title reaction was achieved (se...
A highly regioselective functionalization of indole at the C-4 position by employing an aldehyde fun...
The first example of Rh(III)-catalyzed cyclization of arylnitrones to indolines under external oxida...
Regioselective direct functionalization of an indole benzenoid fragment has been a significant chall...
A general protocol for the synthesis of N-alkyl indoles has been developed via a redox neutral C–H a...
A distinct C–H activation-based traceless synthetic protocol via electrophilic removal of a directin...
A new strategy is reported for the economical synthesis of indoles bearing an <i>N</i>-(3-aminobut-2...
Unprotected indoles are prepared with the title method, which has a wide scope for alkynes. Excellen...
The redox-neutral annulation of alkynes by differently decorated nitrones set the stage for a step-e...
The first Ru-catalyzed redox-neutral C-H activation reaction via N-N bond cleavage is reported. Pyra...
An Efficient Route to 2,3-Disubstituted Indoles via Reductive Alkylation Using H2 as Reductan
Rh-catalyzed redox-neutral coupling between N-aryl nitrones and alkynes has been achieved under rela...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
Versatile nickel catalysts enabled the step-economical synthesis of decorated indoles through alkyne...
An efficient route to 2,3-disubstituted indoles was developed via reductive alkylation of 2-substitu...
Pd doles it out: A palladium-catalyzed approach to indoles using the title reaction was achieved (se...
A highly regioselective functionalization of indole at the C-4 position by employing an aldehyde fun...
The first example of Rh(III)-catalyzed cyclization of arylnitrones to indolines under external oxida...
Regioselective direct functionalization of an indole benzenoid fragment has been a significant chall...