Lewis acid-catalyzed formal (4+2)-cycloaddition between cross-conjugated azatrienes and styrylmalonates: the way to functionalized quinolizidine precursors

HIGHLIGHTS

  • who: Pavel G. Sergeev and colleagues from the Moscow, Russia have published the research work: Lewis Acid-Catalyzed Formal (4+2)-Cycloaddition between Cross-Conjugated Azatrienes and Styrylmalonates: The Way to Functionalized Quinolizidine Precursors, in the Journal: Molecules 2023, 88 of /2023/
  • what: The authors attempted to adapt the previously presented method for the synthesis of tetrahydropyridines to the preparation of potential for these heterocycles as a separate development of a necessary intermediate stage.

SUMMARY

    The authors have recently presented a useful method for highly diastereoselective construction of 1,2,3 . . .

     

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