1140920-60-0Relevant articles and documents
C1-Symmetric aminosulfoximines in copper-catalyzed asymmetric vinylogous mukaiyama aldol reactions
Frings, Marcus,Atodiresei, Iuliana,Wang, Yutian,Runsink, Jan,Raabe, Gerhard,Bolm, Carsten
supporting information; experimental part, p. 4577 - 4587 (2010/08/19)
Vinylogous Mukaiyama-type aldol reactions have been catalyzed by a combination of Cu(OTf)2 and readily available C1-symmetric aminosulfoximines. After a fine-tuning of the reaction conditions and an optimization of the modularly assembled ligand structure, high stereoselectivities and excellent yields have been achieved in catalyzed reactions involving various electrophile/nucleophile combinations. The relative and absolute configurations of two products were assigned by X-ray single crystal structure analysis and a comparison of calculated and experimental CD spectra.