Asymmetric Synthesis, BINAPs, Chemical Synthesis, Chemicals for the synthesis of candidate COVID-19 treatments, Chiral Catalysts, Ligands, and Reagents, Nelfinavir Mesylate, Privileged Ligands and Complexes
1) (R)-BINAP or (R)-Tol-BINAP when combined with dichloro(1,5-cyclooctadiene)ruthenium, form precursors to Noyori Catalyst Systems which exhibit very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. For example, Noyori Catalyst Systems are highly enantioselective in the hydrogenation of functionalized ketones containing dialkylamino, hydroxy, siloxy, carbonyl, ester, amide or thioester substituents (Ref: CHEMTECH, 1992, 360)
2. Useful ligand in asymmetric Heck processes (Ref: Asymmetric Catalysis in Organic Synthesis, 1993, 61)
3. Asymmetric hydroformylation of styrene and vinyl acetate (J. Mol. Catal. A: Chem. 283(1), 15-22, (2008))
|1 gm||In Stock||On Request|
|10 gm||In Stock||On Request|
|50 gm||In Stock||On Request|
|1 kg||4-5 Weeks||On Request|
|25 kg||8-10 Weeks (Negotiable)||On Request|
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