61999-49-3Relevant academic research and scientific papers
Reductive dehalogenation of 4-halogenomethyl azetidin-2-one derivatives. Synthesis of (4-oxo-azetidin-2-yl)acetonitriles
Boros, Eva,Bertha, Ferenc,Fetter, Jozsef,Vida, Laszlo,Kajtar-Peredy, Maria,Czira, Gabor
, p. 558 - 563 (2007/10/03)
The stability of the β-lactam ring under reductive conditions was examined in order to find a selective method for the synthesis of (4-oxo-azetidin-2-yl)acetonitrile derivatives. Fifteen variously substituted 4-halogenomethyl-β-lactam derivatives were syn
Formation of 2,3-Dihydro-4(1H)-quinolones and Related Compounds via Fries-type Acid-catalysed Rearrangement of 1-Arylazetidin-2-ones
Kano, Shinzo,Ebata, Tsutomu,Shibuya, Shiroshi
, p. 2105 - 2111 (2007/10/02)
A variety of 1-arylazetidin-2-ones were treated with trifluoroacetic acid under reflux, methanesulphonic acid at 100 deg C, or conc. sulphuric acid to give the corresponding 2,3-dihydro-4(1H)-quinolones via acyl migration and N-CO fission.In the case of 1-(3-substituted phenyl)azetidin-2-ones, two positional isomeric products, 5- and 7-substituted 2,3-dihydro-4(1H)-quinolones were obtained. 4-Methyl, 4-ethoxycarbonyl, and 4-piperidin-2-yl-1-arylazetidin-2-ones and their analogues were also converted into the corresponding 2-substituted 2,3-dihydro-4(1H)-quinolones under acidic conditions.The 3-substituted 1-phenylazetidin-2-ones (36) and (37) were converted into the furoquinoline systems (38) and (40), respectively, by application of this method.
