Catalytic enantioselective Reformatsky reaction with aldehydes

58Citations
Citations of this article
18Readers
Mendeley users who have this article in their library.
Get full text

Abstract

(Chemical Presented) 120 years after the discovery of the Reformatsky reaction, the first effective catalytic enantioselective Reformatsky reaction with aldehydes using a binol derivative as a chiral catalyst is presented (see scheme; TMS = trimethylsilyl). The reaction is performed with ethyl iodoacetate and Me2Zn. The presence of air is found to be crucial to reach high conversions and selectivities. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.

Cite

CITATION STYLE

APA

Fernández-Ibáñez, M. Á., Maciá, B., Minnaard, A. J., & Feringa, B. L. (2008). Catalytic enantioselective Reformatsky reaction with aldehydes. Angewandte Chemie - International Edition, 47(7), 1317–1319. https://doi.org/10.1002/anie.200704841

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