Asymmetric 1,3-Dipolar Cycloadditons of Stabilized Azomethine Ylides with Nitroalkenes
Jose M. Sansano.
This review highlights the biological importance of many polysubstituted nitro-prolines and -pyrrolidines.
Their preparation using asymmetric 1,3-dipolar cycloadditions of azomethine ylides with nitroalkenes using diastereoselective
and enantioselective strategies is described remarking the scope and main features of each one.
Keywords: Antitumoral, asymmetric synthesis, catalysis, cycloaddition, metal, organocatalyst.
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