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.
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CITATION STYLE
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
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