Highly enantioselective synthesis of Warfarin by primary amine–phosphinamide bifunctional catalysts

This paper is HOT as recommended by the referees, and is free to access for 4 weeks.

In this HOT article Juan Dong and Da-Ming Du, Beijing Institute of Technology, present a new organocatalytic enantioselective Michael addition of 4-hydroxycoumarin to α,β-unsaturated ketones.

The article features a new kind of bifunctional primary amine–phophinamide catalyst, which when applied to catalyze the Michael reaction of 4-hydroxycoumarin to α,β-unsaturated ketones lead to the synthesis of the important pharmaceutical product Warfarin.

Highly enantioselective synthesis of Warfarin and its analogs catalysed by primary amine–phosphinamide bifunctional catalysts

Juan Dong and Da-Ming Du
DOI: 10.1039/C2OB26334C

This article features as part of OBC‘s organocatalysis collection. If you liked this article why not have a look at the collection for other articles on organocatalysis….
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