RESUMO
A novel ruthenium-catalyzed decarboxylative cross-coupling of carbonothioate is disclosed. This method provides straightforward access to the corresponding allyl(aryl)sulfide derivatives in generally good to excellent yields under mild conditions and features a broad substrate scope, wide group tolerance and in particular, no need to use halocarbon precursors.
RESUMO
In the title compound, C(12)H(10)N(2)O, the dihedral angle between the pyridine ring system and the phenyl ring is 1.8â (1)°. There is an intra-molecular N-Hâ¯N hydrogen bond between the pyridine N atom and the amide NH function.
RESUMO
In the title compound, C(17)H(12)O(4), the chromene unit is approximately planar, the maximum deviation from the mean plane being 0.0166â Å. The attached phenyl ring makes a dihedral angle of 53.2â (1)° with the fused ring system. The packing of the mol-ecules in the crystal structure is governed by C-Hâ¯O and O-Hâ¯O hydrogen-bonding inter-actions.