89049-64-9

Upstream product

• 42811-75-6 p-bromobenzonitrile N-oxide 
• 89049-63-8 3-(4-Bromo-phenyl)-5,7a-di-tert-butyl-3a,7a-dihydro-benzo[d]isoxazole-4,7-dione 
• 2460-77-7 2,5-di-tert-butyl-p-benzoquinone 
• 29203-58-5 4-bromo-N-hydroxybenzenecarboximidoyl chloride 

Downstream Products

• 144782-61-6 3,6-Bis-(4-bromo-phenyl)-5-tert-butyl-5-hydroxy-5H-benzo[1,2-d;4,3-d']diisoxazol-4-one 
• 144782-59-2 3-(4-Bromo-phenyl)-6-[3-(4-bromo-phenyl)-5-tert-butyl-4,5-dihydro-isoxazol-4-yl]-6a-tert-butyl-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