| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275592 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
Successful enantioselective Heck-Matsuda arylations were accomplished for the first time using chiral bisoxazolines as ligands. Enantioselective Heck arylations were performed with several cyclic nonactivated olefins to provide the Heck products in 63-96% isolated yields and in enantiomeric excesses of 54% up to 84%.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Carlos Roque D. Correia, Caio C. Oliveira, Airton G. Jr., Emerson A.F. Santos,