International audienceHerein, a direct C8‐arylation reaction of 1‐amidonaphthalenes is described. By using diaryliodonium salts as arylating agents, the palladium‐catalyzed C−H activation reaction showed perfect C8 regioselectivity and a wide functional group tolerance. In most cases, the desired polyaromatic compounds were isolated in good to excellent yields. To explain the observed regioselectivity, DFT calculations were performed and highlighted the crucial role of the amide directing group. Finally, the utility of this method is showcased by the synthesis of benzanthrone derivatives
A palladium(II)-catalyzed quinolinamide-directed 8-arylation of 1-naphthylamides with aryl iodides ...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
International audienceHerein, a direct C8‐arylation reaction of 1‐amidonaphthalenes is described. By...
International audienceHerein, a direct C8‐arylation reaction of 1‐amidonaphthalenes is described. By...
International audienceHerein, a direct C8‐arylation reaction of 1‐amidonaphthalenes is described. By...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
A palladium(II)-catalyzed quinolinamide-directed 8-arylation of 1-naphthylamides with aryl iodides ...
A palladium(II)-catalyzed quinolinamide-directed 8-arylation of 1-naphthylamides with aryl iodides ...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
International audienceHerein, a direct C8‐arylation reaction of 1‐amidonaphthalenes is described. By...
International audienceHerein, a direct C8‐arylation reaction of 1‐amidonaphthalenes is described. By...
International audienceHerein, a direct C8‐arylation reaction of 1‐amidonaphthalenes is described. By...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
International audienceHerein, a direct C8-oxygenation of naphthalene derivatives is described. Diffe...
A palladium(II)-catalyzed quinolinamide-directed 8-arylation of 1-naphthylamides with aryl iodides ...
A palladium(II)-catalyzed quinolinamide-directed 8-arylation of 1-naphthylamides with aryl iodides ...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...