PdII/PdIV Catalytic Enantioselective Synthesis of Bicyclo[3.1.0]hexanes via Oxidative Cyclization of Enynes

102Citations
Citations of this article
42Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The first asymmetric PdII/PdIV catalysis has been achieved by employing the combination of a hypervalent iodine reagent and a chiral ligand, SPRIX. Enantioselective cyclization of enyne derivatives catalyzed by the Pd-i-Pr-SPRIX complex furnished lactones bearing a bicyclo[3.1.0]hexane skeleton with up to 95% ee. Copyright © 2009 American Chemical Society.

Cite

CITATION STYLE

APA

Tsujihara, T., Takenaka, K., Onitsuka, K., Hatanaka, M., & Sasai, H. (2009). PdII/PdIV Catalytic Enantioselective Synthesis of Bicyclo[3.1.0]hexanes via Oxidative Cyclization of Enynes. Journal of the American Chemical Society, 131(10), 3452–3453. https://doi.org/10.1021/ja809965e

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