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|Type:||Artigo de periódico|
|Title:||The First Examples Of The Enantioselective Heck-matsuda Reaction: Arylation Of Unactivated Cyclic Olefins Using Chiral Bisoxazolines|
Salles Jr. A.G.
|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%. © 2012 Elsevier Ltd. All rights reserved.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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