Catalytic Enantioselective [3+2] Cycloaddition of N-Metalated Azomethine Ylides

36Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Asymmetric [3+2] cycloaddition reactions are fascinating and powerful methods for the synthesis of enantioenriched pyrrolidines up to four stereocentres. Pyrrolidines are important compounds for both biology and organocatalytic applications. This review summarizes the most recent advances in the enantioselective synthesis of pyrrolidines by [3+2] cycloadditions of azomethine ylides using metal catalysis. It has been organized by the type of metal catalysis used and further arranged by the complexity nature of dipolarophile. The presentation of each reaction type highlights their advantages and limitations.

Cite

CITATION STYLE

APA

Kumar, S. V., & Guiry, P. J. (2023, May 16). Catalytic Enantioselective [3+2] Cycloaddition of N-Metalated Azomethine Ylides. Chemistry - A European Journal. John Wiley and Sons Inc. https://doi.org/10.1002/chem.202300296

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free