35392-44-0

Upstream product

• 103-26-4 methyl cinnamate 
• 1137-96-8 N-(benzylidene)aniline N-oxide 
• 19713-73-6 methyl (2Z)-3-phenylprop-2-enoate 
• 201024-81-9 C,N-diphenylnitrone 
• 103-26-4 Methyl cinnamate 

Relevant academic research and scientific papers

Remarkable stereocontrol in 1,3-dipolar cycloaddition of acyclic nitrones: Investigation of the cycloaddition of C,N-diaryl nitrones to methyl cinnamate under different reaction conditions

Investigation of the cycloaddition of C,N-diarylnitrones to methyl cinnamate under different reaction conditions were carried out. Two diastereoisomeric and one regioisomeric cycloadducts were isolated and characterized by spectroscopic and X-ray data. Re

[3+2] cycloadditions: Part XXXIV: Further investigations of cycloadditions of C,N-diaryl- and C-aryl-N-methyl nitrones to α,β-unsaturated esters

Investigations of [3+2] cycloadditions of C,N-diaryl and C-aryl-N-methyl nitrones as three atom components (TAC) to substituted methyl E-cinnamates and diethyl arylidene malonates have been further investigated. [3+2] Cycloadditions of cinnamates yielded mixtures of cycloadducts, the major products being the 3,4-trans-4,5-trans-2,3,5-triaryl-4-carbomethoxy products originating from the endo-carbonyl-exo-aryl meta channel approach of the cinnamate component. [3+2] Cycloadditions to diethyl arylidene malonates furnished single cycloadducts-3,5-trans-2-methyl-3,5-diaryl-4,4-dicarbethoxy isoxazolidines by a endo-aryl meta channel approach of the 2π-component.