Multicomponent Radical Processes: Synthesis of Substituted Piperidinones
Journal of the American Chemical Society2007Vol. 129(42), pp. 12662–12663
Citations Over TimeTop 10% of 2007 papers
Abstract
Three and four-component radical and radical−organometallic processes have been developed that provide a simple access to 2,3-disubstituted piperidinones. Reasonable yield and high stereoselectivities were achieved in a number of cases with three C−C bonds and one C−N bond and up to three stereogenic centers generated in one pot from readily available reagents.
Related Papers
- → Resolution/Deracemization of Chiral α-Amino Acids Using Resolving Reagents with Flexible Stereogenic Centers(2009)95 cited
- → Asymmetric Silaboration of Terminal Allenes Bearing α-Stereogenic Centers: Stereoselection Based on “Reagent Control”(2006)53 cited
- → Dibenzylamine substituted cyclotetraphosphazenes: Synthesis, characterization and their stereogenic properties(2018)5 cited
- → Reversal of enantioselectivity using catalysts containing multiple stereogenic centres(2001)34 cited
- → 2.4 General Principles of Diastereoselective Reactions: Acyclic Control of Diastereoselectivity(2012)1 cited