Recyclable fluorous cinchona organocatalysts for asymmetric synthesis of biologically interesting compounds

Organocatalysis has unique modes of activation, mild reaction conditions, and good catalyst structural amenability. The integration of green techniques such as catalyst recovery and one-pot reactions makes organocatalysis more efficient and attractive. Presented in this article are the recyclable cinchona alkaloid-catalyzed reactions including fluorination and Michael addition-initiated cascade reactions in asymmetric synthesis of functionalized compounds of biological interest.

Automated summary

Organocatalysis offers unique activation modes, mild reaction conditions, and good catalyst adaptability, making it more efficient with the integration of green techniques. This article focuses on recyclable cinchona alkaloid-catalyzed reactions in the asymmetric synthesis of functionalized compounds of biological interest.