Issue 32, 2014

Cu(i)/TF–BiphamPhos-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides with dimethyl itaconate and 2-methyleneglutarate

Abstract

Catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides with dimethyl itaconate and 2-methyleneglutarate was realized with the Cu(I)/TF–BiphamPhos complex as the catalyst for the efficient construction of pyrrolidine derivatives bearing one unique all carbon-quaternary and two tertiary stereogenic centers. The current catalytic system exhibited excellent diastereoselectivity (> 20 : 1), good enantioselectivity (88–>99% ee) and broad substrate scope under mild conditions.

Graphical abstract: Cu(i)/TF–BiphamPhos-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides with dimethyl itaconate and 2-methyleneglutarate

Supplementary files

Article information

Article type
Paper
Submitted
07 Feb 2014
Accepted
25 Mar 2014
First published
27 Mar 2014

RSC Adv., 2014,4, 16899-16905

Author version available

Cu(I)/TF–BiphamPhos-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides with dimethyl itaconate and 2-methyleneglutarate

H. Tao, Z. He, Y. Yang and C. Wang, RSC Adv., 2014, 4, 16899 DOI: 10.1039/C4RA02195A

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