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A convenient regioselective synthesis of spirooxindolinopyrrolizidines incorporating the pyrene moiety through a [3 + 2]-cycloaddition reaction

Research Abstract

A facile one-pot synthesis of spirooxindolinopyrrolizidines incorporating the pyrene moiety was accomplished in good yields through a 1,3-dipolar cycloaddition reaction of 3-aryl-1-(pyren-1-yl)prop-2-en-1-one derivatives with in situ-generated azomethine ylides.

Research Date
Research Department
Research Journal
Heterocyclic Communications
Research Publisher
Walter de Gruyter GmbH
Research Rank
Q2
Research Vol
Volume 23
Research Website
https://doi.org/10.1515/hc-2017-0036
Research Year
2017