|Related Categories||Asymmetric Synthesis, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, MacMillan Imidazolidinone OrganoCatalysts|
Used in the 1,4-addition of electron-rich benzenes to unsaturated aldehydes, and the asymmetric hydride reduction of α,β-unsaturated aldehydes.1,2
1 g in glass bottle
500 mg in glass bottle
U.S. Pat. 6,369,243 and related patents apply. For research purposes only.
Customers Also Viewed
MacMillan and co-workers have created chiral imidazolidinone organocatalysts that function as the linchpin in a variety of directed enantioselective organic reactions including Diels–Alder and 1,3-di...
Aldrich ChemFiles 2006, 6.7, 11.
Keywords: Addition reactions, Alkylations, Asymmetric synthesis, Chlorinations, Cycloadditions, Epoxidations, Fluorinations, Hydrogenations, Organocatalysis
MacMillan and co-workers have created chiral imidazolidinone organo-catalysts that function as the linchpin in a variety of directed enantioselective organic reactions, including the enamine-catalyze...
Aldrich ChemFiles 2006, 6.2, 9.
Keywords: 1,3-Dipolar cycloaddition, Asymmetric synthesis, Catalysis, Chlorinations, Cycloadditions, Fluorinations, Natural product synthesis
Developed by Professor David MacMillan at Caltech, imidazolidinone-based OrganoCatalysts™ are designed to serve as general catalysts for a variety of asymmetric transformations. The first highly enan...
Keywords: Alkylations, Asymmetric catalysis, Asymmetric synthesis, Catalysis, Chlorinations, Condensations, Cycloadditions, Diels-Alder reaction, Fluorinations, Friedel-Crafts Alkylation
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Need larger quantities for your development, manufacturing or research applications?