26463-62-7Relevant articles and documents
Reactions of diphenacylaniline and diphenacyl sulfide under Gewald conditions: Generation of enamines and thioamides
Paul, Nidhin,Sathishkumar, Ramalingam,Anuba, Chellathurai,Muthusubramanian, Shanmugam
, p. 7445 - 7451 (2013/06/27)
The 1,5-diketone, diphenacylaniline, yielded an enamine under Gewald conditions, while another 1,5-diketone, diphenacyl sulfide, resulted in thioamide formation under identical conditions. 2-Amino-4-(3-oxo-1,3- diphenylpropyl)-4,5,6,7-tetrahydrobenzo[b]th
Tribenzoyldihydropyridinols from dibenzoylacetylene and imines
Gomaa, Mohsen Abdel-Motaal
, p. 81 - 83 (2007/10/03)
The reaction of dibenzoylacetylene with N,N′-dialkyl or N,N′-diaryl glyoxal-bisimnes or with benzylideneanilines in boiling ethanol leads to the formation of pentasubstituted 1,2-dihydropyridines in 52-87% yield together with the corresponding enamines derived from dibenzoylacetylene.
Reactions of aromatic nitro compounds with acetophenone in the presence of alkali. Crystal structure of (E)-1,2-dibenzoyl-o-tolylaminoethylene
Greci, Lucedio,Pieroni, Mirco,Tosi, Giorgio,Rizzoli, Corrado,Sgarabotto, Paolo,Ugozzoli, Franco
, p. 693 - 699 (2007/10/02)
Methyl and methoxy substituted nitroarenes were reacted with acethophenone in the presence of sodium ethoxide in ethanol giving arylamino-conjugated diketo derivatives.A case of ipso-substitution of a methoxy group is discussed.The title compound C23H19NO