89049-62-7

Upstream product

• 2460-77-7 2,5-di-tert-butyl-p-benzoquinone 
• 28123-63-9 4-chlorobenzohydroximoyl chloride 

Downstream Products

• 144782-62-7 5-tert-Butyl-3,6-bis-(4-chloro-phenyl)-5-hydroxy-5H-benzo[1,2-d;4,3-d']diisoxazol-4-one 
• 144782-60-5 6a-tert-Butyl-6-[5-tert-butyl-3-(4-chloro-phenyl)-4,5-dihydro-isoxazol-4-yl]-3-(4-chloro-phenyl)-6-hydroxy-6,6a-dihydro-3aH-furo[3,4-d]isoxazol-4-one 

Relevant academic research and scientific papers

The Reactions of Nitrile Oxide-Quinone Cycloadducts. II. The Reactions of 2,5-Di-t-butyl-p-benzoquinone with Nitrile Oxides: 1:2 Cycloaddition and Base Induced Ring Transformation of the Cycloadducts.

The reactions of 2,5-di-t-butyl-p-benzoquinone with p-substituted benzonitrile N-oxides successfully gave 1:2 cycloadduct.The cycloadducts were proved to undergo base induced reactions in different patterns with aqueous sodium hydroxide or with triethylam

The Reaction of Nitrile Oxides with Alkyl- and Alkyl-halo-substituted p-Benzoquinones

Various aromatic nitrile N-oxides, sterically stabilized and unstabilized ones, were allowed to react with several alkyl- and alkyl-halo-substituted p-benzoquinones with a view to studying the influence of quinone substituents on the mode of the addition