127311-22-2

Upstream product

• 3212-60-0 cyclopent-2-enol 
• 27143-81-3 tert-butyl nitrile oxide 
• 98-88-4 benzoyl chloride 
• 3551-51-7 N-(cyclopent-2-en-1-yl)-benzamide 
• 3350-06-9 2-cyclopentenamine 
• 127311-07-3 6-benzamido-3-tert-butyl-3aα,5,6α,6aα-tetrahydro-4H-cyclopentisoxazole 
• 74-88-4 methyl iodide 
• 127310-74-1 N-(cyclopent-2-en-1-yl)-N-methylbenzamide 
• 3273-26-5 1-chloro-2,2-dimethyl-propan-1-one oxime 
• 127311-07-3 6-benzamido-3-tert-butyl-3aα,5,6β,6aα-tetrahydro-4H-cyclopentisoxazole 

Relevant academic research and scientific papers

HYDROGEN BOND DIRECTED NITRILE OXIDE CYCLOADDITION REACTIONS OF ALLYLIC 2o-AMIDES

The ability of allylic and homoallylic 2o-amides to direct nitrile oxide cycloaddition reactions has been studied.For N-cyclopentenyl amides, good regio- and stereochemical control are observed and mechanistic studies suggest that hydrogen bond

Directed Nitrile Oxide Cycloaddition Reactions. The Use of Hydrogen Bonding To Direct Regio- and Stereochemistry in Nitrile Oxide Cycloadditions with Cyclopentenylamides

2 deg amides derived from cyclopentenylamine direct the regio- and stereochemistry of cycloaddition reactions with benzonitrile oxide and 2,2-dimethylpropane nitrile oxide by hydrogen bonding.