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  • Cu(I)-catalyzed highly exo-selective and enantioselective [3 + 2] cycloaddition of azomethine ylides with acrylates.

Cu(I)-catalyzed highly exo-selective and enantioselective [3 + 2] cycloaddition of azomethine ylides with acrylates.

Organic letters (2005-09-09)
Wenzhong Gao, Xumu Zhang, Malati Raghunath
ABSTRACT

[reaction: see text] A novel Cu(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides with acrylates has been developed. Up to 98/2 exo/endo selectivity and up to 98% enantiomeric excess have been achieved.

MATERIALS
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Brand
Product Description

Sigma-Aldrich
Glycine methyl ester hydrochloride, 99%