Mild and efficient synthesis of ynones via Ir(III)- and Rh(III)-catalyzed, chelation-assisted formyl C–H alkynylation of benzaldehydes has been achieved using hypervalent iodine–alkyne reagents. Rhodium and iridium catalysis exhibited complementary substrate scope
The C–H heteroarylation of benzaldehydes with indoles and pyrroles was realized using the benziodoxo...
Transition metal-catalyzed carbon–carbon (C–C) bond activation is a useful way to construct organic ...
An efficient C–H activation method for the <i>ortho</i> alkynylation of aromatic <i>N-</i>methoxyami...
Mild and efficient synthesis of ynones via Ir(III)- and Rh(III)-catalyzed, chelation-assisted formyl...
Mild and efficient synthesis of benzophenones via Ir(III)- and Rh(III)catalyzed, directing group-ass...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C–H alkynylation of a broad scope ...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C–H alkynylation of a broad scope ...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C H alkynylation of a broad scope of...
Rh(III)-catalyzed efficient C-H alkynylation of azomethine imines with alkynylated hypervalent iodin...
The rhodium(III)-catalyzed ortho C[BOND]H alkynylation of non-electronically activated arenes is dis...
Formal regiodivergent C–H alkynylation of 2-pyridones bearing different <i>N</i>-substituents has be...
Formal regiodivergent C-H alkynylation of 2-pyridones bearing different N-substituents has been real...
The rhodium(I)-catalyzed reaction of alkynes with arylboronic acids in the presence of formaldehyde ...
An Ir‐catalyzed C(sp3)−H alkynylation of aliphatic ketones, aldehydes, and alcohols was achieved by ...
The C–H heteroarylation of benzaldehydes with indoles and pyrroles was realized using the benziodoxo...
The C–H heteroarylation of benzaldehydes with indoles and pyrroles was realized using the benziodoxo...
Transition metal-catalyzed carbon–carbon (C–C) bond activation is a useful way to construct organic ...
An efficient C–H activation method for the <i>ortho</i> alkynylation of aromatic <i>N-</i>methoxyami...
Mild and efficient synthesis of ynones via Ir(III)- and Rh(III)-catalyzed, chelation-assisted formyl...
Mild and efficient synthesis of benzophenones via Ir(III)- and Rh(III)catalyzed, directing group-ass...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C–H alkynylation of a broad scope ...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C–H alkynylation of a broad scope ...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C H alkynylation of a broad scope of...
Rh(III)-catalyzed efficient C-H alkynylation of azomethine imines with alkynylated hypervalent iodin...
The rhodium(III)-catalyzed ortho C[BOND]H alkynylation of non-electronically activated arenes is dis...
Formal regiodivergent C–H alkynylation of 2-pyridones bearing different <i>N</i>-substituents has be...
Formal regiodivergent C-H alkynylation of 2-pyridones bearing different N-substituents has been real...
The rhodium(I)-catalyzed reaction of alkynes with arylboronic acids in the presence of formaldehyde ...
An Ir‐catalyzed C(sp3)−H alkynylation of aliphatic ketones, aldehydes, and alcohols was achieved by ...
The C–H heteroarylation of benzaldehydes with indoles and pyrroles was realized using the benziodoxo...
The C–H heteroarylation of benzaldehydes with indoles and pyrroles was realized using the benziodoxo...
Transition metal-catalyzed carbon–carbon (C–C) bond activation is a useful way to construct organic ...
An efficient C–H activation method for the <i>ortho</i> alkynylation of aromatic <i>N-</i>methoxyami...
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