- Substituted Sulfonamide Compounds
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Substituted sulfonamide compounds corresponding to the formula I: processes for the preparation thereof, pharmaceutical composition containing these compounds and the use of substituted sulfonamide compounds for the preparation of pharmaceutical compositions.
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Page/Page column 43
(2009/10/17)
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- Substituted Sulfonamide Compounds
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Substituted sulfonamide compounds corresponding to formula I pharmaceutical compositions comprising them, a process for preparing them, and the use of such compounds to treat or inhibit pain and other disorders or disease states.
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Page/Page column 36
(2009/01/24)
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- Quinazoline deriviates for treating peptic ulcer
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A quinazoline derivative represented by formula(I) or a pharmaceutically acceptable salt thereof is useful for the treatment of peptic ulcer, wherein: STR1 R1 and R2 are each hydrogen or a C1 -C4 alkyl group; R3 is hydrogen or a halogen; R4, R5, R6, R7, R8 and R9, which may be the same or different, are each hydrogen, a C1 -C4 alkyl group, a cyclopropyl group, or a C1 -C4 alkyl group substituted with a halogen; and R10 is a methoxy group.
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- Synthesis of the Marine Alkaloids Aaptamine and Demethyloxyaaptamine and of the Parent Structure Didemethoxyaaptamine
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The first synthesis of the novel marine alkaloids aaptamine and demethyloxyaaptamine is described, as well as the first synthesis of the parent heterocycle 1H-benzonaphthyridine (didemethoxyaaptamine).
- Pelletier, Jeffrey C.,Cava, Michael P.
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p. 616 - 622
(2007/10/02)
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- The Reaction of 3,4-Dihydroisoquinolines With Malonic Acid and Its Derivatives
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The reaction of various 3,4-dihydroisoquinolines with malonic acid gives the corresponding 1,2,3,4-tetrahydro-1-isoquinolineacetic acids in good yield, while the reaction with cyanoacetic acid and malonic acid half ethyl ester affords 1,2,3,4-tetrahydro-1
- Pelletier, Jeffrey C.,Cava, Michael P.
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p. 474 - 477
(2007/10/02)
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