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Enantioselective Nazarov Cyclizations Catalyzed by an Axial Chiral C6F5‐Substituted Boron Lewis Acid
Authors:Lars Süsse  Maria Vogler  Dr. Marius Mewald  Dr. Benedict Kemper  Dr. Elisabeth Irran  Prof. Dr. Martin Oestreich
Affiliation:1. http://www.organometallics.tu‐berlin.de 0000-0002-4894-1198 Institut für Chemie, Technische Universit?t Berlin, Berlin, Germany;2. Institut für Chemie, Technische Universit?t Berlin, Berlin, Germany;3. Organisch-Chemisches Institut, Westf?lische Wilhelms-Universit?t Münster, Münster, Germany
Abstract:A chiral variant of B(C6F5)3 with a 3,3′‐disubstituted binaphthyl backbone is shown to catalyze Nazarov cyclizations with high levels of enantio‐ and diastereocontrol. The parent B(C6F5)3 also promotes these ring closures efficiently. This electrocyclization is another example of the still small family of C?C bond formations mediated by B(C6F5)3 as the catalyst.
Keywords:asymmetric catalysis  boron  C−  C bond formation  electrocyclic reactions  Lewis acids
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