Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...
Reexamination Certificate
2006-04-11
2006-04-11
Solola, Taofiq (Department: 1626)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Having -c-, wherein x is chalcogen, bonded directly to...
C504S266000, C548S202000, CD22S120000
Reexamination Certificate
active
07026341
ABSTRACT:
The present invention relates to new hetaryl-substituted homotetramic and homotetronic acids of the formula (I)in whichA, B, Q1, Q2, W, G and Het have the meanings stated in the disclosure,to a plurality of processes for their preparation, and to their use as pesticides, microbicides, and herbicides.
REFERENCES:
patent: 3538107 (1970-11-01), Hepworth et al.
patent: 3749787 (1973-07-01), Hepworth et al.
patent: 5084083 (1992-01-01), Lewis et al.
patent: 5789440 (1998-08-01), Ellsworth et al.
patent: 5840751 (1998-11-01), Ellsworth et al.
patent: 5936128 (1999-08-01), Ellsworth et al.
patent: 6028033 (2000-02-01), Hill et al.
patent: 6071937 (2000-06-01), Bretschneider et al.
patent: 0 328 954 (1989-08-01), None
patent: 0 885 885 (1998-12-01), None
patent: 8-325230 (1996-12-01), None
patent: 11-152273 (1999-06-01), None
Djudjic et al., Org. Preparations and Procedures Intl., (1985), vol. 17, No. 3, pp. 206-210.
Lacan et al., Acta Pharmaceutical Jugoslavica, (1981), vol. 31, No. 1, pp. 47-51.
Arch. Pharm. 309, (month unavailable) 1976, pp. 558-565, “Zur Synthese von Kawalactonderivaten” by A. M. Chirazi et al.
J. Amer. Chem. Soc., 93, Jan. 31, 1971, pp. 281-282, “Darzens Condensation of α-Haloactones: Glycidic Lactones as Intermediates in Acetogenin Synthesis” by J. D. White et al.
Chemical Reviews, vol. 52, (month unavailable) 1953, pp. 237-416.
Indian J. Chem, vol. 6, Jul. 1968, pp. 341-345, Isoquinoline Derivates: Part XVIII-Formation of I-Alkyl-(or Alkaryl or aryl)-3-methyl-7-chloro-(or 5-chloro)-isoquinolines by B. Bhattacharya.
Chem. Ind (London), Nov. 9, 1968, p, 1568, “Use of molecular sieves in the methyl esterification of carboxylic acids” by H. R. Harrison et al.
Organikum [Organic Chemistry], VEB Deutcher Verlag der Wissenschaften, (month unavailable) Berlin 1977, pp. 505-507, D.7.1.5. Reaktionen von Carbonsäuren und Carbonsäurederivaten mit Basen.
H. Henecka, Houben-Weyl, Methoden der Organischen Chemie, [Methods in Organic Chemistry], (month unavailable) 1952, vol. 8, pp. 467-469, “Isoanthraflavinsäure; Morpholchinon”.
Chem. Parm. Bull. 46 (7), pp. 1116-1124, (month unavailable) 1998, “Novel 5-Hydroxytryptamine 4 (5-HT4) Receptor Agonist Synthesis and Gastroprokinetic Activity of 4-Amino-M-[2-(1-aminocycloalkan-1-yl)ethyl]-5-chloro-2-methoxybenzamides” by T. Suzuki et al.
Organikum, VEB Deutscher Verlag der Wissenschaften, (month unavailable) Berlin 1990, 18th ed. pp. 501-502, “D.7.3.5. Reaktionen mit metallorganischen Verbindungen”.
Chem. Ind., 37, (month unavailable) 1985, pp. 730-732, “Schiffsfarben—eine Spezialitäder seenahen Lackindustrie” by H. R. Ungerer.
J. Med. Chem., (month unalailable) 1983, 26, pp. 700-714, “Inhibitors of Glycolic Acid Oxidase. 4-Substituted 3-Hydroxy-1H-pyrrole-2,5-dione Derivatives” by C. S. Rooney et al.
J. Med. Chem. (month unavailable) 1996, 39, pp. 237-245, “Azole Phenoxy Hydroxyureas as Selective and Orally Active Inhibitors of 5-Lipoxygenase” by M. S. Malamas.
J. Med. Chem., (month unavailable) 1998, 41, pp. 5037-5054,N-(2-Benzoylphenyl)-L-tyrosine PPARy Agonists. 1. Structure-Activity Relationship and Opitimization of the Phenyl Alkyl Ether Moiety by J. L. Collins et al.
Synthetic Communications, 28(4), pp. 701-712, (month unavailable) 1998, “Synthesis Of Novel Restricted Diamines; 2-(1-Aminocycloalkan-1-YL)Ethylamines” by T. Suzuki et al.
Justus Liebigs Ann. Chem., 661, (month unavailable) 19631 pp. 111-157, “Umsetzungen Mit Olefinen Und Aldehyden; Uber β-Lactame” by von Roderich Graf.
Dahmen Peter
Drewes Mark Wilhelm
Erdelen Christoph
Feucht Dieter
Fischer Reiner
Bayer CropScience AG
Harmuth Raymond J.
Henderson Richard E. L.
Solola Taofiq
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