1441-42-5

Upstream product

• 6271-22-3 1,5-diphenyl-4-pentene-1,3-dione 
• 873-67-6 benzonitrile oxide 
• 5622-76-4 1-phenylbut-1-en-3-yne 
• 1008-74-8 5-methyl-3-phenylisoxazole 
• 538-51-2 benzylidene phenylamine 
• 614-57-3 1,5-diphenylpenta-2,4-dien-1-one 
• 103-36-6 ethyl 3-phenyl-2-propenoate 
• 146537-63-5 1,5-diphenyl-2,4-pentadien-1-one oxime 
• 98-86-2 acetophenone 

Relevant academic research and scientific papers

TBAI-catalyzed intramolecular annulation of chalcone oximes toward isoxazoles

A TBAI-catalyzed intramolecular annulation of chalcone oximes toward isoxazoles was developed, providing 3,5-diarylisoxazoles in good yields. Functional groups such as methoxy, ethyoxyl, chloro, bromo, fluoro and nitro were well tolerated in this reaction

Copper-catalyzed aerobic oxidative C-O bond formation for the synthesis of 3,5-disubstituted isoxazoles from enone oximes

A direct access to 3,5-disubstituted isoxazoles has been accomplished through an intramolecular oxidative coupling reaction of enone oximes using a catalytic quantity of Cu(OAc)2. This method features an inexpensive metal catalyst, molecular ox

A novel and convenient method for the synthesis of 3, 5-diarylisoxazoles

α,β-Unsaturated oximes of chalcones on treatment with 2,3-Dichloro- 5,6-dicyano-1,4-benzoquinone (DDQ) in methanol furnish 3,5-disubstituted isoxazoles in good yield.

A convenient preparation of 3,5-diarylisoxazoles

3,5-Diarylisoxazoles 2a-i were prepared in moderate to high yields 51-94%) by oxidation of chalcone oximes with a new metal complex oxidant, tetrakis(pyridine)cobalt(II) dichromate (TPCD).