Affiliation:
1. Institute of Organic Chemistry, Faculty of Chemistry Lodz University of Technology Żeromskiego 116, Łódź 90-924, Poland
Abstract
The allylic alkylation of indene-2-carbaldehydes with Morita–Baylis–Hillman (MBH) carbonates via pentaenolate activation is described. High stereoselectivities of the process rely on the use of a chiral tertiary amine as a nucleophilic catalyst.
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis
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