Coumarin compounds and method for preparing and using the same

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C549S289000, C549S290000

Reexamination Certificate

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11273372

ABSTRACT:
4-Substituted coumarin compounds having the general formula ofwhere R is H, CHO, OCH3, X, NO2, an alkyl having C1-10, —OCH2O—, an aryl being mono- or poly-substituted with CN or COOCH3with the aryl being a phenyl, naphthyl, or azaryl, or a coumarin groupthat is substituted with R1, R2, R3, R4, with R1, R2, R3, and R4being H, an alkyl having C1-10, X, NO2, CN, OCH3, COOCH3or OR5, R5being H or an alkyl having C1-10, and X being a halogen.

REFERENCES:
patent: 4083857 (1978-04-01), Townend et al.
patent: 5554611 (1996-09-01), Schonafinger et al.
patent: 02-191269 (1990-07-01), None
patent: 2876129 (1999-01-01), None
patent: WO9804572 (1998-02-01), None
patent: WO9825608 (1998-06-01), None
Pillon et al., Bull. Soc. Chim., “Derivatives of flavones. III. Synthesis of polyhydroxy flavones”, 1954, pp. 9-25.
Gogte et al., Physical Sciences, Mathematics, Biological Sciences and Medicine, “Elimination of Acetic acid during decarboxylation of organic acids part III. A new synthesis of 4-aryl-coumarins from B, B'-diarylglutaromonolactonic acids”, 1959, vol. 27, pp. 6-13.
Saxena et al., Proceedings of the National Academy of Sciences, India, Section A: Physical Sciences, “A new 4-phenylcoumarin “Sisafolin” fromDalbergia Latifolia”, 1970, vol. 40(pt. 2), pp. 165-169.
Tickle et al., Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-organic Chemistry, “Intraction of Gringnard reagents with coumarins. I. Novel 1,40addition”, 1974, vol. 5, pp. 569-574.
Chawla et la., Bulletin de la Societe Chimique de France, “New Phenolic coponents fromDalbergia volubilis”, 1989, vol. 1, pp. 82-87.
Zou et al., Yaoxue Xuebao, “Structure determination of inflacoumarin A fromGlycyrrhiza inflata”, 1994, vol. 29, pp. 397-399.
Zou et al., Journal of Chinese Pharmaceutical Sciences, “Constituents fromGlycyrrhiza inflataand antioxidant activities of phenols from the roots ofGlycyrrhiza”, 1994, vol. 3, p. 90.
Yianbin et al., Bopuxue Zazhi, “NMR study of inflacoumarin A”, 1994, vol. 11, pp. 399-403.
Wu et al., Tetrahedron Letters, “Palladium-catalyyzed cross-coupling reactions of 4-tosyloxycoumarin and arylboronic acids: synthesis of 4-arylcoumarin compounds”, 2002, vol. 43, pp. 4395-4397.
Garazd et al., Chemistry of Natural Compounds (Translation of Khimiya Prirodnykh Soedinenii), Modified Coumarins. 8. Synthesis of substituted 5-(4-Methoxyphenyl)-7H-furo[3,2-g]chromen-7-ones, 2002, vol. 38, pp. 539-548.
Lei Jianguang et al., The first total systhesis of 4, 4-bisisofraxidin, Chinese J. Chem., (2002), 20, 1263-1267, the whole document.
Pharkphoom P. et al.; “a new biscoumarin from impatiens balsamina root cultures”, Planta Medica, (1998), 64, 774-775, compound 1.
Paradkar M. V. et al.; “a facile synthesis of new [4, 4-bi-2H-1-benzopyran]-2, 2-diones”, Synthetic Communications, (1988), 18(6), 589-596, 1, compound 3a-c.
Zhang yanying et al., “a study on the synthesis and spectra characteristics of coumarins”, Dyestuffs and Coloration, (2002), 40 (2), 68-70, the whole document.
Min-liang Yao et al., “a novel and convenient method to 4-substituted coumarins”, Heteroatom Chem., (2000), 11(6), 380-382, table 1.
Laurent Schio et al., “tosylates in palladium-catalysed coupling reactions. Application to synthesis of arylcoumarin inhibitors of gyrase B”, Tetrahedron Lett., (2000), 41, 1543-1547, table 1.
Jayati et al., “Palladium in organic synthesis: Part IV palladium (0) catalyzed arylation of coumarin”, Indian J. Chem., (1996), 35B, 588-589, table 1.
Bose et al., “synthesis of 4-phenylcoumarins”, Indian J. Chem., (1990), 29B , 422-424, table 1.
Dervilla, “a new approach to neoflavonoid synthesis”, J. Chem. Soc. Perkin Trans., (1990), 1, 2851-2852, table 1.
Zhang yanying et al., “current development in synthetic methods for arylcoumarins”, Dyestuffs and Coloration, (2002), 40 (1), 39-41, the whole document.
Mohammad e tal., “biomimetic synthesis of some novel coumarin dimers”, Tetrahedron, (1996), 52(11), 3991-3996.
Johannes, “synthesis of the natural coumarins (E)-suberenol, cyclobisuberodiene and two other related new coumarins”, J. Reisch, Natural Products Chem., (1990), 139, 931-933.
Soroush et al., “synthesis and antifungal activity of coumarins and angular furanocoumarins”, Bioorg. Med. Chem., (1999), 7, 1933-1940.
Hao xiaojiang et al., “the chemical constituents of boenninghausenia sessilicarpa”, Acta Botanica Yunnanica, (1994), 16(3), 310-312.
Zhao yajun et al., “a reverse friedel-crafts reaction and the synthesis of enzo[h]coumarin”, Acta Scientiarum Naturalium Universitatis Perkinensis, (1994), 30 (4), 421-424.

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