79894-87-4

Upstream product

• 21572-32-7 2-chloro-1-phenyl-ethanone oxime 
• 542-92-7 cyclopenta-1,3-diene 

Downstream Products

• 130223-59-5 (5aR,8aS)-1-Oxy-9a-phenyl-3,5a,8,8a,9,9a-hexahydro-cyclopenta[e]imidazo[1,2-b][1,2]oxazine-2-carbaldehyde 
• 130223-61-9 12-formyl-9-phenyl-2,10-dioxa-1,11-diazatricyclo-<7.4.0.0^3,7>trideca-4,11-diene 
• 130223-62-0 12-acetyl-9-phenyl-2,10-dioxa-1,11-diazatricyclo-<7.4.0.0^3,7>trideca-4,11-diene 
• 83670-30-8 (5aS,8aR,9aS)-2,9a-Diphenyl-3,5a,8,8a,9,9a-hexahydro-cyclopenta[e]imidazo[1,2-b][1,2]oxazine 1-oxide 
• 128710-04-3 cis-4-Methyl-4,4a,5,7a-tetrahydro-3-phenylcyclopent-1,2-oxazine 
• 128779-03-3 trans-4-Methyl-4,4a,5,7a-tetrahydro-3-phenylcyclopent-1,2-oxazine 
• 128710-06-5 4-<(1-Hydroxy-1-methyl)ethyl>-4,4a,5,7a-tetrahydro-3-phenylcyclopent-1,2-oxazine 
• 128710-03-2 C₁₃H₁₂⁽²⁾HNO 
• 128779-02-2 C₁₃H₁₂⁽²⁾HNO 
• 125781-47-7 5-(2-Phenylamino-ethyl)-cyclopent-2-enol 
• 125781-41-1 trans-1,2,3,3a,4,6a-hexahydro-1-hydroxy-2-phenylcyclopentapyrrole 
• 130223-58-4 (5aR,8aS)-2-(4-Nitro-phenyl)-9a-phenyl-3,5a,8,8a,9,9a-hexahydro-cyclopenta[e]imidazo[1,2-b][1,2]oxazine 1-oxide 
• 130223-60-8 12-p-nitrophenyl-9-phenyl-2,10-dioxa-1,11-diazatricyclo-<7.3.0.0^3,7>trideca-4,11-diene 
• 128710-05-4 cis-4-Methylthio-4,4a,5,7a-tetrahydro-3-phenylcyclopent-1,2-oxazine 

Relevant academic research and scientific papers

Nitrosoalkenes: Synthesis and Reactivity

Some α- and β-halonitrosoalkenes 1 have been synthesized and characterized.The halogen atoms of the oxime precursors 2 can be substituted by alkoxy groups.Two kinds of cycloaddition reaction of 1 have been observed: i) reaction of the NO group with dienes