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Catalyzed Vinylogous Mukaiyama Aldol Reactions with Controlled Enantio- and Diastereoselectivities

✍ Scribed by Marcus Frings; Iuliana Atodiresei; Jan Runsink; Gerhard Raabe; Carsten Bolm


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
198 KB
Volume
15
Category
Article
ISSN
0947-6539

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## Abstract Vinylogous Mukaiyama‐type aldol reactions have been catalyzed by a combination of Cu(OTf)~2~ and readily available __C__~1~‐symmetric aminosulfoximines. After a fine‐tuning of the reaction conditions and an optimization of the modularly assembled ligand structure, high stereoselectiviti