- Full text PDF available (1)
- This year (0)
- Last 5 years (0)
- Last 10 years (1)
Journals and Conferences
The reaction of dimethyl acetylenedicarboxylate (DMAD) with 2-naphthol in the presence of trimethyl or triphenyl phosphite leads to stable dimethyl oxa-2 lambda 5-phosphaphenanthrene derivatives in good yields. The reaction of DMAD and trimethyl phosphite in the presence of 1-naphthol or 8-hydroxyquinoline leads to dimethyl… (More)
The reaction of dibenzoylacetylene and enaminocarbonyl compounds leads to 3-alkylidene-2,3-dihydro-1H-pyrrol-2-ol derivatives in nearly quantitative yields. The reaction of this heterocyclic system with alcohols in the presence of a catalytic amount of HCl produces highly functionalized pyrroles in good yields.
The adducts produced in the reaction between triphenylphosphine and dialkyl acetylenedicarboxylates were trapped by arylsulfonyl isocyanates to produce dialkyl 2,5-dihydro-5-oxo-1,2-azaphosphole-3,4-dicarboxylates in good yields.
In the title compound, C(16)H(18)N(2)O(6), the dihedral angle between the aromatic ring planes is 8.11 (6)°. One of the O atoms is disordered over two sites of equal occupancy. In the crystal structure, aromatic π-π stacking [centroid-to-centroid separation = 3.5503 (8) Å] helps to consolidate the packing.