Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acid esters
Reexamination Certificate
2007-09-03
2011-12-13
Zucker, Paul A (Department: 1621)
Organic compounds -- part of the class 532-570 series
Organic compounds
Carboxylic acid esters
C562S015000
Reexamination Certificate
active
08076503
ABSTRACT:
The present invention is a process for producing optically active aminophosphinylbutanoic acids represented by the formula (2),comprising asymmetrically hydrogenating a compound represented by the formula (1)in the presence of a ruthenium-optically active phosphine complex, a process for the production thereof, and a compound useful in a herbicide such as L-AHPB that can be produced with good efficiency and high asymmetric yield.
REFERENCES:
patent: 4168963 (1979-09-01), Rupp et al.
patent: 4499027 (1985-02-01), Minowa et al.
patent: 4777279 (1988-10-01), Zeiss
patent: 4922006 (1990-05-01), Zeiss
patent: 6313317 (2001-11-01), Sayo et al.
patent: 6686181 (2004-02-01), Bartsch
patent: 6936444 (2005-08-01), Bartsch
patent: 52-139727 (1977-11-01), None
patent: 55-00025 (1980-01-01), None
patent: 59-219297 (1984-12-01), None
patent: 62-132891 (1987-06-01), None
patent: 62-226993 (1987-10-01), None
patent: 11-269185 (1999-10-01), None
patent: 2003-505031 (2003-02-01), None
patent: 2003-528572 (2003-09-01), None
patent: 2004/035594 (2004-04-01), None
H. Zeiss, “An Efficient Asymmertric Synthesis of Both Enantiomers of Phosphinothricin”, Tetrahedron Letters, vol. 28, No. 12, pp. 1255-1258, 1987.
H. Zeiss, “Enantioselective Synthesis of L-Phosphinothricin from L-Methionine and L-Glutamic Acid via L-Vinylglycine”, Tetrahedron, vol. 48, No. 38, pp. 8263-8270, 1992.
H. Zeiss, “Enantioselective Synthesis of Both Enantiomers of Phosphinothricin via Asymmetric Hydrogenation of α-Acylamido Acrylates”, J. Org. Chem., vol. 56, No. 5, pp. 1783-1788, 1991.
W. Tang et al., “New Chiral Phosphorus Ligands for Enantioselective Hydrogenation”, Chem. Rev., vol. 103, No. 8, pp. 3029-3069, 2003.
T. Ikariya et al.,“Synthesis of Novel Chiral Ruthenium Complexes of 2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl and Their Use as Asymmetric Catalyst”, J. Chem. Soc., Chem. Commun., pp. 922-924, 1985.
K. Mashima et al., “Synthesis of New Cationic BINAP-Ruthenium(II) Complexes and Their Use in Asymmetric Hydrogenation [BINAP = 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl]”, J. Chem. Soc., Chem. Commun., pp. 1208-1210, 1989.
Extended European Search Report issued Mar. 3, 2011 in European Application No. 07806589.3.
M. Kitamura et al., “Mechanism of Asymmetric Hydrogenation of α-(Acylamino)acrylic Esters Catalyzed by BINAP-Ruthenium(II) Diacetate”, J. Am. Chem. Soc., vol. 124, No. 23, pp. 6649-6667, Jun. 12, 2002.
Minowa Nobuto
Mitomi Masaaki
Nakanishi Nozomu
Nara Hideki
Yokozawa Tohru
Meiji Seika Pharma Co., Ltd.
Takasago International Corporation
Wenderoth , Lind & Ponack, L.L.P.
Zucker Paul A
LandOfFree
Process for production of optically active... does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Process for production of optically active..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Process for production of optically active... will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-4295494