Inventor
SAYO NOBORU
JP50 patents
⚠️ This page may combine multiple inventors who share the name “SAYO NOBORU”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.
TAKASAGO PERFUMERY CO LTD
49 patentsUS5206399AApr 27, 1993
2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl and transition metal complex containing the same as ligand
TAKASAGO PERFUMERY CO LTD28 citations93
US5847222ADec 8, 1998
Optically active diphosphine compound, method for making the compound, transition metal complex having the compound as ligand and method for making optically active substance by use of the complex
TAKASAGO PERFUMERY CO LTD22 citations92
US5530150AJun 25, 1996
Phosphine compound, complex containing the phosphine compound as ligand, process for producing optically active aldehyde using the phosphine compound or the complex, and 4-[(R)-1'-formylethyl]azetidin-2-one derivatives
TAKASAGO PERFUMERY CO LTD23 citations92
US4994590AFeb 19, 1991
Ruthenium-phoshine complex
TAKASAGO PERFUMERY CO LTD27 citations92
US4962230AOct 9, 1990
Process for producing optically active carboxylic acid
TAKASAGO PERFUMERY CO LTD25 citations92
US4739084AApr 19, 1988
Ruthenium-phosphine complex
TAKASAGO PERFUMERY CO LTD45 citations92
US7964744B2Jun 21, 2011
Method for producing a ruthenium complex
TAKASAGO PERFUMERY CO LTD9 citations84
US6333291B1Dec 25, 2001
Optically active diphosphine compound, production intermediate thereof, transition metal complex containing the compound as ligand and asymmetric hydrogenation catalyst containing the complex
TAKASAGO PERFUMERY CO LTD17 citations83
US5693868ADec 2, 1997
Method for producing optically active diphosphine compounds
TAKASAGO PERFUMERY CO LTD18 citations82
US4916252AApr 10, 1990
Process for preparing optically active alcohol
TAKASAGO PERFUMERY CO LTD21 citations82
US4994602AFeb 19, 1991
Process for preparing optically active 6-t-butyoxy-3,5-dihydroxyhexanoic esters
TAKASAGO PERFUMERY CO LTD21 citations81
US4739085AApr 19, 1988
Ruthenium-phosphine complex
TAKASAGO PERFUMERY CO LTD22 citations80
US5066815ANov 19, 1991
Process for preparing optically active alcohol
TAKASAGO PERFUMERY CO LTD20 citations79
US4981992AJan 1, 1991
Process for preparing optically active 3-hydroxybutanoic acid
TAKASAGO PERFUMERY CO LTD21 citations79
US6492545B2Dec 10, 2002
Process for producing optically active alcohol
TAKASAGO PERFUMERY CO LTD12 citations74
US4933482AJun 12, 1990
Process for preparing optically active alcohol
TAKASAGO PERFUMERY CO LTD18 citations74
US6342644B1Jan 29, 2002
Method for producing 1-menthol
TAKASAGO PERFUMERY CO LTD13 citations73
US6313317B1Nov 6, 2001
Ruthenium-phosphine complex and method for producing the same
TAKASAGO PERFUMERY CO LTD10 citations73
US5808162ASep 15, 1998
Chiral unsymmetric diphosphine compound and transition metal complex containing the same as ligand
TAKASAGO PERFUMERY CO LTD12 citations73
US5789609AAug 4, 1998
Optically active diphosphine, transition metal complex containing the same, and process for producing optically active compound using the complex
TAKASAGO PERFUMERY CO LTD11 citations73
US5563295AOct 8, 1996
Process for producing optically active carboxylic acid
TAKASAGO PERFUMERY CO LTD8 citations73
US5502221AMar 26, 1996
Process for producing cyclohexylbutyric acid derivative
TAKASAGO PERFUMERY CO LTD6 citations73
US5420306AMay 30, 1995
Process for producing optically active γ-butyrolactone derivatives
TAKASAGO PERFUMERY CO LTD12 citations73
US4962242AOct 9, 1990
Process for producing optically active alcohols
TAKASAGO PERFUMERY CO LTD17 citations73
US4766227AAug 23, 1988
Ruthenium-phosphine complex
TAKASAGO PERFUMERY CO LTD14 citations73
US4766225AAug 23, 1988
Ruthenium-phosphine complex
TAKASAGO PERFUMERY CO LTD15 citations73
US4764629AAug 16, 1988
Ruthenium-phosphine complex
TAKASAGO PERFUMERY CO LTD7 citations73
US5616751AApr 1, 1997
Oxotitanium complex, asymmetric hydrogenation catalyst comprising the complex, and process for producing β-hydroxy ketone or α-hydroxy carboxylic acid ester using the complex
TAKASAGO PERFUMERY CO LTD7 citations72
US5922918AJul 13, 1999
Method for making an optically active diphosphine ligand
TAKASAGO PERFUMERY CO LTD9 citations70
US4954644ASep 4, 1990
Ruthenium-phosphine complex
TAKASAGO PERFUMERY CO LTD18 citations69
US6040465AMar 21, 2000
Process for producing optically active β-lactones
TAKASAGO PERFUMERY CO LTD10 citations68
US7754889B2Jul 13, 2010
Optically active transition metal-diamine compound and process for producing optically active alcohol with the same
TAKASAGO PERFUMERY CO LTD5 citations63
US4965398AOct 23, 1990
Process for producing optically active alpha-hydroxycarboxylates
TAKASAGO PERFUMERY CO LTD3 citations63
US6465594B1Oct 15, 2002
Phosphine derivative and polymer thereof and transition metal complex comprising the same
TAKASAGO PERFUMERY CO LTD3 citations62
US5442105AAug 15, 1995
Process for producing cyclohexylbutyric acid derivative
TAKASAGO PERFUMERY CO LTD2 citations62
US5434289AJul 18, 1995
Process for producing optically active β-hydroxyketone
TAKASAGO PERFUMERY CO LTD2 citations62
US5324870AJun 28, 1994
Process for producing optically active 1-substituted-1,3-propanediols using ruthenium-phosphine complex as a catalyst
TAKASAGO PERFUMERY CO LTD3 citations62
US5286888AFeb 15, 1994
Ruthenium-phosphine complex and process for producing optically active 1-substituted-1,3-propanediols using the same as a catalyst
TAKASAGO PERFUMERY CO LTD4 citations62
US6472539B1Oct 29, 2002
Production process of diphosphine oxide and diphosphonate
TAKASAGO PERFUMERY CO LTD2 citations61
US5523458AJun 4, 1996
Process for producing optically active diaminohexanone derivative
TAKASAGO PERFUMERY CO LTD3 citations61
US5198562AMar 30, 1993
Ruthenium-phosphine complex and intermediate for producing the same
TAKASAGO PERFUMERY CO LTD3 citations61
US5919962AJul 6, 1999
Process for preparing ruthenium-phosphine complex
TAKASAGO PERFUMERY CO LTD2 citations60
US7294601B2Nov 13, 2007
Phosphines, transition metal complexes containing the same as the ligand, and process for production of optically active carboxylic acids
TAKASAGO PERFUMERY CO LTD0 citations52
US5714624AFeb 3, 1998
Oxotitanium complex, asymmetric hydrogenation catalyst comprising the complex, and process for producing β-hydroxy ketone or α-hydroxy carboxylic acid ester using the complex
TAKASAGO PERFUMERY CO LTD0 citations51
US5705678AJan 6, 1998
Oxotitanium complex, asymmetric hydrogenation catalyst comprising the complex, and process for producing β-hydroxy ketone or α-hydroxy carboxylic acid ester using the complex
TAKASAGO PERFUMERY CO LTD0 citations51
US5631397AMay 20, 1997
Process for producing optically active diaminohexanone derivative
TAKASAGO PERFUMERY CO LTD1 citations51
US6596887B2Jul 22, 2003
Process for producing an optically active ruthenium-phosphine complex and process for producing an optically active alcohol by using the complex
TAKASAGO PERFUMERY CO LTD1 citations47
US5155240AOct 13, 1992
Process for producing optically active dihydropyran derivative
TAKASAGO PERFUMERY CO LTD0 citations42
US5581007ADec 3, 1996
Process for preparing optically active allophenylnorstatin derivatives
TAKASAGO PERFUMERY CO LTD0 citations41