1283128-83-5Relevant academic research and scientific papers
Dipolar cycloaddition of N-aryl-C-(2,2-dichloro-1-phenylcyclopropyl) nitrones to N-arylmaleimides
Molchanov,Sorokoumov,Kopf,Kostikov
, p. 66 - 73 (2011)
1,3-Dipolar cycloaddition of N-aryl-C-(2,2-dichloro-1-phenylcyclopropyl) nitrones to N-arylmaleimides stereoselectively gives substituted pyrrolo[3,4-d]isoxazolidines as mixtures of two diastereoisomers differing by configuration at the C1′ atom of the cyclopropane ring in the substituent on C3. Substituents in the aromatic rings of the initial nitrone and maleimide do not affect the stereochemistry of the process.
