Convergent Catalysis: Asymmetric Synthesis of Dihydroquinolines Using a Combined Metal Catalysis and Organocatalysis Approach
ACS Catalysis2014Vol. 4(3), pp. 1021–1025
Citations Over TimeTop 10% of 2014 papers
Abstract
A convergent catalysis approach has been developed. The combined metal-catalyzed and organocatalyzed cascade consists of two oxidations, an aza-Michael addition and an aldol condensation, and involves a multicatalysis approach to provide 1,2-dihydroquinolines in a highly enantioselective fashion.
Related Papers
- → Solvent-Free Enantioselective Organocatalyzed Aldol Reactions(2014)17 cited
- → A short and efficient synthesis of N-Cbz-galantinic acid under promoter control on enantioselective acyclic stereoselection based on chiral oxazaborolidinone-promoted aldol reactions(2000)22 cited
- → Remarkable long range effects on the diastereoface selectivity in an aldol condensation(1999)16 cited
- → Aldol Reaction and Aldol Condensation(2010)
- → Asymmetric aldol reactions(1996)