Herein we report a novel iridium(III)-catalyzed ortho-mono-alkynylation of 7-azaindoles under mild conditions. This approach provides a general and straightforward access to form novel 7-azaindole derivatives with ample substrate scope and broad group tolerance.National Science Foundation of China [21172011]SCI(E)EIPubMedARTICLElirt@bjmu.edu.cn102944-29491
The ruthenium(II)-catalyzed C–H aminocarbonylation of <i>N</i>-(hetero)aryl-7-azaindoles with isoc...
Mild and efficient synthesis of ynones via Ir(III)- and Rh(III)-catalyzed, chelation-assisted formyl...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
Rhodium(III)-catalyzed double C–H activation involving <i>N</i>-directed <i>ortho</i> C–H activatio...
An efficient Rh(III)-catalyzed 7-azaindole synthesis was developed via C-H activation/annulative cou...
A Rh(III)-catalyzed C-H ortho-mono-olefination of aryls directed by 7-azaindoles was reported. This ...
An iridium-catalyzed direct C-7 selective C–H alkynylation of indolines at room temperature, for the...
A convenient and practical approach to synthesize <i>ortho</i>-alkynylated arylalkylamines through <...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C H alkynylation of a broad scope of...
The Rh(III)-catalyzed ortho-alkynylation of benzaldehydes is enabled by the transient formation of a...
Selective C–H bond alkynylation toward modular access to material and pharmaceutical molecules is of...
Iridium-catalyzed regioselective C-7 amination of indolines has been achieved with organic azides as...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C–H alkynylation of a broad scope ...
A modular, regioselective, step-economical, and chelation-assisted dehydrogenative alkynylation of c...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C–H alkynylation of a broad scope ...
The ruthenium(II)-catalyzed C–H aminocarbonylation of <i>N</i>-(hetero)aryl-7-azaindoles with isoc...
Mild and efficient synthesis of ynones via Ir(III)- and Rh(III)-catalyzed, chelation-assisted formyl...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...
Rhodium(III)-catalyzed double C–H activation involving <i>N</i>-directed <i>ortho</i> C–H activatio...
An efficient Rh(III)-catalyzed 7-azaindole synthesis was developed via C-H activation/annulative cou...
A Rh(III)-catalyzed C-H ortho-mono-olefination of aryls directed by 7-azaindoles was reported. This ...
An iridium-catalyzed direct C-7 selective C–H alkynylation of indolines at room temperature, for the...
A convenient and practical approach to synthesize <i>ortho</i>-alkynylated arylalkylamines through <...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C H alkynylation of a broad scope of...
The Rh(III)-catalyzed ortho-alkynylation of benzaldehydes is enabled by the transient formation of a...
Selective C–H bond alkynylation toward modular access to material and pharmaceutical molecules is of...
Iridium-catalyzed regioselective C-7 amination of indolines has been achieved with organic azides as...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C–H alkynylation of a broad scope ...
A modular, regioselective, step-economical, and chelation-assisted dehydrogenative alkynylation of c...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C–H alkynylation of a broad scope ...
The ruthenium(II)-catalyzed C–H aminocarbonylation of <i>N</i>-(hetero)aryl-7-azaindoles with isoc...
Mild and efficient synthesis of ynones via Ir(III)- and Rh(III)-catalyzed, chelation-assisted formyl...
Rh(III)-catalyzed regioselective alkylation of indoles with diazo compounds as a highly efficient an...