A mild, regioselective, iridium-catalyzed C–H amidation and borylation of anthraquinones to the o-sulfonamide and m-borylated products has been developed. The anthraquinone carbonyl moieties direct the C–H amidation with high selectivity to afford the ortho-substituted products in modest to high yields
Iridium catalysed C-H borylation has moved from an interesting observation to an efficient catalytic...
Direct C–H borylation of hexa-<i>peri</i>-hexabenzocoronenes (HBCs) has been achieved under iridium ...
The preformed catalyst [Ir(Cl)(COD)(1,10-phenanthroline)] (<b>2</b>; COD = cyclooctadiene) was fo...
Reported is an iridium catalyst for ortho-selective C-H borylation of challenging secondary aromatic...
An iridium-catalyzed C–H borylation provides the key step in a short synthesis of two indolequinone ...
Ir-catalyzed direct C–H sulfamidation of benzaldehydes has been achieved. A series of <i>ortho</i>-a...
Transition metal catalysed C-H activation is a highly desirable strategy for the functionalization o...
An iridium-catalyzed regioselective C-H borylation of pentafluoroaniline-derived heteroaromatic aldi...
International audienceAn efficient iridium-catalyzed C(sp2)−H reaction of non-aromatic tertiary enam...
Iridium-catalyzed direct ortho C–H amidation of arenes has been shown to work well with sulfonyl- an...
A study on the iridium-catalyzed C–H borylation of heteroarenes is reported. Several heteroarenes co...
A convenient and practical approach to synthesize <i>ortho</i>-alkynylated arylalkylamines through <...
The iridium-catalyzed arene C–H borylation reaction of benzylic amines has been developed, which inv...
Iridium-catalyzed direct ortho C-H amidation of arenes has been shown to work well with sulfonyl- an...
The hemilabile character of 2-pyridyl carbaldehyde hydrazones as N,N bidentate ligands is key to per...
Iridium catalysed C-H borylation has moved from an interesting observation to an efficient catalytic...
Direct C–H borylation of hexa-<i>peri</i>-hexabenzocoronenes (HBCs) has been achieved under iridium ...
The preformed catalyst [Ir(Cl)(COD)(1,10-phenanthroline)] (<b>2</b>; COD = cyclooctadiene) was fo...
Reported is an iridium catalyst for ortho-selective C-H borylation of challenging secondary aromatic...
An iridium-catalyzed C–H borylation provides the key step in a short synthesis of two indolequinone ...
Ir-catalyzed direct C–H sulfamidation of benzaldehydes has been achieved. A series of <i>ortho</i>-a...
Transition metal catalysed C-H activation is a highly desirable strategy for the functionalization o...
An iridium-catalyzed regioselective C-H borylation of pentafluoroaniline-derived heteroaromatic aldi...
International audienceAn efficient iridium-catalyzed C(sp2)−H reaction of non-aromatic tertiary enam...
Iridium-catalyzed direct ortho C–H amidation of arenes has been shown to work well with sulfonyl- an...
A study on the iridium-catalyzed C–H borylation of heteroarenes is reported. Several heteroarenes co...
A convenient and practical approach to synthesize <i>ortho</i>-alkynylated arylalkylamines through <...
The iridium-catalyzed arene C–H borylation reaction of benzylic amines has been developed, which inv...
Iridium-catalyzed direct ortho C-H amidation of arenes has been shown to work well with sulfonyl- an...
The hemilabile character of 2-pyridyl carbaldehyde hydrazones as N,N bidentate ligands is key to per...
Iridium catalysed C-H borylation has moved from an interesting observation to an efficient catalytic...
Direct C–H borylation of hexa-<i>peri</i>-hexabenzocoronenes (HBCs) has been achieved under iridium ...
The preformed catalyst [Ir(Cl)(COD)(1,10-phenanthroline)] (<b>2</b>; COD = cyclooctadiene) was fo...
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