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History of Takasago Fine Chemicals Division
Takasago has a history of over a quarter century in asymmetric synthesis and our challenge to create new technologies will continue.

1980 Professor Ryoji Noyori’s group developed BINAP catalyst.
Asymmetric isomerization of allylamine by Rh-BINAP complex.
Asymmetric synthesis of l-menthol.
1983 Commercial production of BINAP by optical resolution.
The first industrial asymmetric isomerization, l-menthol.
1984 Asymmetric hydrogenation of dehydroamino acids by Ru-BINAP complex.
1988 Asymmetric hydrogenation of ß-ketoesters by Ru-BINAP complex.
1989 Dynamic kinetic resolution.
4-Acetoxy azetidinone, 4-AA process.
1992 Commercial production of chiral 1,2-propanediol.
1993 Commercial production of 4-AA.
1994 Hydroformylation ligands, BINAPHOS and BIPNITE.
1995 Noyori reduction, RuCl2(diphosphine)(diamine) system.
1996 Asymmetric transfer hydrogenation, RuCl(arene)(sulfonylated diamine) system.
SEGPHOS® , advanced-BINAP ligand.
2001 Professor Ryoji Noyori, a board member of Takasago, received the Nobel Prize.
BRIDP, advanced ligands for Pd-Coupling.
2002 Received Molecular Chirality Award, “Development of SEGPHOS”.
2003 Reductive amination for ß-amino acid.
2005 Cu mediated asymmetric hydrogenation.
2006 Received Merck’s Suppliers’ Award.
2007 Received Tetrahedron Most Cited Paper 2004-2007 Award, “Recent Advances in Biaryl-Type Bisphosphine Ligands”.
Hydrogenation of esters by homogeneous catalyst .
2008 Received Tetrahedron Most Cited Paper 2005-2008 Award, “Recent Advances in Biaryl-Type Bisphosphine Ligands”.
2009 Received Poster Award at 2009’s OMCOS in Glasgow, “An Efficient Synthesis of Chiral Alcohols via Catalytic Hydrogenation of Esters”.
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