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Articles
Asymmetric Conjugate Addition
In the past 5 years, chiral diene ligands have surfaced for a variety of asymmetric transformations. Hayashi1 and Carreira2 pioneered this field by synthesizing chiral diene ligands that formed stabl...
William Sommer
Aldrich ChemFiles 2008, 8.6, 11.
Keywords: Addition reactions, Arylations, Asymmetric synthesis, Building blocks, Catalysis, Ligands
Asymmetric Hydrosilylation
The asymmetric hydrosilylation of olefins has proven to be a useful method to access a variety of chiral alcohols.1 The introduction of the silica moiety allows further transformation of the molecule...
William Sommer
Aldrich ChemFiles 2008, 8.6, 4.
Keywords: Asymmetric synthesis, Hydrosilylations, Ligands, transformation
Carreira DOLEFIN Ligands
For the past years, the Carreira group has been employing chiral [2.2.2]bicyclooctadienes derived from (R)- or (S)-carvone in Ir(I)-catalyzed kinetic resolution of allylic carbonates1 and Rh(I)-catal...
Aldrich ChemFiles 2006, 6.10, 4.
Keywords: Addition reactions, Asymmetric synthesis, Catalysis, Infrared spectroscopy, Ligands
Palladium-Catalyzed Reduction of Allylic Esters
The palladium catalyzed reduction of allylic esters provides a convenient method to access chiral olefins.1Hayashi et al. studied the activity of the MOP ligand with palladium toward the reduction of...
William Sommer
Aldrich ChemFiles 2008, 8.6, 4.
Keywords: Catalysis, Ligands, Reductions
Papers
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1. Tetrahedron 63, 12961, (2007)
Fieser 5,203
Aldrich MSDS 1, 640:D / Corp MSDS 1 (1), 1168:A / FT-IR 2 (3), 4512:C / FT-IR 1 (2), 1236:B / RegBook 1 (2), 3075:A / Structure Index 1, 487:B:7