34310-06-0

Upstream product

• 1201-93-0 1-phenyl-3-dimethylaminoprop-2-enone 
• 2904-57-6 mesitylenecarbonitrile oxide 
• 40685-20-9 (E)-3-methoxy-1-phenylprop-2-en-1-one 
• 127703-96-2 Phenyl-[3-(2,4,6-trimethyl-phenyl)-4,5-dihydro-isoxazol-4-yl]-methanone 
• 2904-63-4 2,4,6-trimethylbenzohydroximoyl chloride 
• 3623-15-2 phenyl propargyl ketone 
• 19968-09-3 3-mesityl-4,5-dihydroisoxazole 
• 93-89-0 benzoic acid ethyl ester 
• 100-52-7 benzaldehyde 
• 127704-03-4 Phenyl-[3-(2,4,6-trimethyl-phenyl)-4,5-dihydro-isoxazol-4-yl]-methanol 
• 127704-00-1 1,1-Bis-[3-(2,4,6-trimethyl-phenyl)-4,5-dihydro-isoxazol-4-yl]-ethanol 
• 768-03-6 Phenyl vinyl ketone 
• 127703-97-3 Phenyl-bis-[3-(2,4,6-trimethyl-phenyl)-4,5-dihydro-isoxazol-4-yl]-methanol 

Relevant academic research and scientific papers

1,3-Dipolar Cycloaddition Reactions of Nitrile Oxides and Nitrile Imines with 2-Methoxyvinyl Phenyl Ketone

Nitrile oxides react regioselectively with 2-methoxyvinyl phenyl ketone 1 to give 4-benzoylisoxazoles 4 via elimination of methanol from the primary cycloadducts 3.After heating with an excess of nitrile oxide bis-cycloadducts 5 were also formed.Reactions

Some Acylations of 3-Phenyl and 3-Mesityl-4,5-dihydroisoxazoles

A study on the acetylation and benzoylation of title compounds by quenching the corresponding 4-carbanions with acyl chlorides or esters is reported.The obtained ketones are formed as minor regioisomeric adducts in the cycloadditions of benzo and mesitoni