European Journal of Organic Chemistry · 2008 · 76 citations · 48 references
Natural SciencesChemical EngineeringChemistryCatalysisOrganic ChemistryReaction EngineeringCatalyst DesignCatalyst PreparationCatalyst SynthesisCatalytic MaterialsHeterocyclic ChemistryOrganic SynthesisCatalyst Development For SynthesisCatalyst Structure - Activity RelationshipsCatalytic ActivityCatalytic Process OptimizationCatalytic Reaction MechanismsChiral Catalyst Design
Abstract A series of chiral substituted 5‐(pyrrolidin‐2‐yl)tetrazoles have been synthesized and evaluated as organocatalysts for the asymmetric Biginelli reaction. The relationship between catalytic activity and the different catalyst structures is briefly discussed. By using the optimized catalyst C 10 (10 mol‐%), a series of 3,4‐dihydropyrimidin‐2(1 H )‐one (DHPM) derivatives have been obtained in 63–88 % yields and 68–81 % ee values within 24 h at room temperature. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
48
100 years of the biginelli dihydropyrimidine synthesis
C. Oliver Kappe · Tetrahedron · 1993 · 1.2K citations
Organocatalytic Direct Asymmetric Aldol Reactions in Water
Nobuyuki Mase, Yusuke Nakai, Naoko Ohara et al. · Journal of the American Chemical Society · 2005 · 650 citations
Organocatalytic Direct Asymmetric Aldol Reactions in Water.
Nobuyuki Mase, Yusuke Nakai, Naoko Ohara et al. · ChemInform · 2006 · 558 citations