125160-90-9Relevant academic research and scientific papers
Synthesis and biological evaluation of fluoro-substituted spiro-isoxazolines as potential anti-viral and anti-cancer agents
Boone, Sarah,Das, Prasanta,Hamme, Ashton T.,Mitra, Dipanwita,Raucher, Drazen,Tandon, Ritesh,Turner, Lindsay
, p. 30223 - 30237 (2020/09/03)
Electrophilic fluorine-mediated dearomative spirocyclization has been developed to synthesize a range of fluoro-substituted spiro-isoxazoline ethers and lactones. The in vitro biological assays of synthesized compounds were probed for anti-viral activity
Larvicidal isoxazoles: Synthesis and their effective susceptibility towards Aedes aegypti larvae
Da Silva-Alves, Diana C.B.,Dos Anjos, Janaina V.,Cavalcante, Nery N.M.,Santos, Geanne K.N.,Navarro, Daniela M.Do A.F.,Srivastava, Rajendra M.
, p. 940 - 947 (2013/03/14)
Twenty 3,5-disubstituted isoxazoles have been synthesized and tested against fourth instar Aedes aegypti larvae. In the synthesis of title compounds, modifications have been made in the C-5 side-chain with a view to test their larvicidal activity. These i
Beyond azide-alkyne click reaction: Easy access to 18F-labelled compounds via nitrile oxide cycloadditions
Zlatopolskiy, Boris D.,Kandler, Rene,Kobus, Diana,Mottaghy, Felix M.,Neumaier, Bernd
supporting information; experimental part, p. 7134 - 7136 (2012/07/27)
Radiofluorinated 4-fluorobenzonitrile oxide and N-hydroxy-4- fluorobenzimidoyl chloride rapidly react with different alkenes and alkynes under mild conditions. These cycloadditions are suitable for the preparation of low-molecular weight radiopharmaceutic
Synthetic applications of 6-hydroxy-1-arylhexane-1,3-diones
De, Dibyendu,Seth, M.,Bhaduri, A. P.
, p. 503 - 506 (2007/10/02)
Facile synthesis of (E)-2-(aroylmethylene)tetrahydrofurans (17-19), 3-aryl-5-(γ-hydroxypropyl)isoxazoles (5-7), 6-hydroxy-1-aryl-3-substitutedaminohex-2-ene-1-ones (14-16), 3-cyano-6-hydroxy-1-arylhex-2-ene-1-ones (23-25) and one pot synthesis of 2-(α-phe
