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. 2007 Nov 7;5(21):3531-4.
doi: 10.1039/b712396e. Epub 2007 Sep 27.

Rh-catalyzed highly enantioselective formation of functionalized cyclopentanes and cyclopentanones

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Rh-catalyzed highly enantioselective formation of functionalized cyclopentanes and cyclopentanones

Fei Liu et al. Org Biomol Chem. .

Abstract

A catalyst system, [Rh(COD)Cl](2)-BINAP-AgSbF(6), has been developed as a second-generation catalyst for the cycloisomerization of 1,6-enynes tethered by carbon chains. Cyclopentanes and cyclopentanones, which can contain functional groups, such as the 1,4-dienes, vinyl ether, aldehyde etc., were obtained from readily available starting materials in high yields and selectivities. Both regioselectivities and enantioselectivities are excellent: only 1,4-dienes were observed and in over 99% ee.

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