Catalytic Asymmetric Synthesis with Rh−Diene Complexes:  1,4-Addition of Arylboronic Acids to Unsaturated Esters

Jean‐François Paquin, Corey R. J. Stephenson, Christian Defieber, Erick M. Carreira

Organic Letters · 2005 · 155 citations · 22 references

Concepts

Abstract

A general route to enantioenriched tert-butyl 3,3-diarylpropanoates is presented. These useful building blocks are prepared via an asymmetric rhodium-catalyzed conjugate addition of arylboronic acids to unsaturated tert-butyl esters in the presence of chiral dienes as ligands. The addition of both electron-poor and electron-rich boronic acids proceeds smoothly with various enoates in 63-90% yield with high enantioselectivites (89-94% ee). [reaction: see text]

References

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