92511-69-8

Upstream product

• 7063-95-8 acetonitrile-N-oxide 
• 98-83-9 isopropenylbenzene 
• 92511-69-8 3,5-Dimethyl-5-phenyl-4,5-dihydro-isoxazole 

Downstream Products

• 92511-79-0 (R)-5-Methyl-5-phenyl-3-((R)-toluene-4-sulfinylmethyl)-4,5-dihydro-isoxazole 
• 92511-80-3 (S)-5-Methyl-5-phenyl-3-((R)-toluene-4-sulfinylmethyl)-4,5-dihydro-isoxazole 
• 92511-69-8 3,5-Dimethyl-5-phenyl-4,5-dihydro-isoxazole 
• 15121-66-1 4-hydroxy-4-phenylpentan-2-one 
• 15121-66-1 4-Hydroxy-4-phenyl-2-pentanone 

Relevant academic research and scientific papers

Synthesis of some isoxazolines and evaluation of carbon-13 NMR substituent parameters for 5-methyl substitution

Some isoxazolines substituted at C-5 with phenyl and methoxycarbonyl groups have been synthesised and characterised.Carbon-13 NMR methyl substituent parameters for methyl substitution at C-5 carbon in these compounds have been evaluated.

Enantiomerically Pure Sulphinyl-4,5-dihydroisoxazoles. Part 1. Stereocontrolled Synthesis of Optically Active β-Ketols and γ-Amino Alcohols

exo-Metallation of racemic 3-methyl-4,5-dihydroisoxazoles and reaction of the products with (-)-(S)-menthyl toluene-p-sulphinate afforded diastereoisomeric 3-sulphinylmethyl derivatives which can be separated and individually converted either into the cor

Synthesis of Enantiomerically Pure Δ2-Isoxazolines via Sulphinyl Derivatives

Optically active 3-sulphinylmethyl-Δ2-isoxazolines allow an easy entry to enantiomerically pure Δ2-isoxazolines and to the corresponding β-hydroxy ketones.