Results 171 to 180 of about 6,842 (226)

Hydrodenitrogenation of isoquinoline

Applied Catalysis A: General, 1999
Abstract To determine the formation and reactivity of addition compounds produced during hydrodenitrogenation (HDN), we investigated the HDN of isoquinoline for a sulfided Ni–Mo/Al 2 O 3 catalyst operated under a hydrogen pressure of 12 MPa (cold charge) in the temperature range 300–375°C.
Yasuo Miki, Yoshikazu Sugimoto
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CXXII.—isoQuinoline and the isoquinoline-reds

J. Chem. Soc., Trans., 1922
John Edmund Guy Harris, William Jackson Pope   +1 more
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Isoquinoline

Acta Crystallographica Section C Crystal Structure Communications, 1999
K. Hensen, R. Mayr-Stein, M. Bolte
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Arsenicals in the Isoquinoline Series

Journal of the American Chemical Society, 1946
B, ELPERN, C S, HAMILTON
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Quinolines and isoquinolines

1992
This chapter assesses quinolines and isoquinolines. Quinoline and isoquinoline are two isomeric heterocyclic systems, which can be envisaged as being constructed from the fusion of a benzene ring at the C2/C3 and C3/C4 positions of pyridine respectively. They are both ten π-electron aromatic heterocycles.
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Isoquinolines

1979
Maurice Shamma, David M. Hindenlang
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Some Substituted Isoquinolines

Journal of the American Chemical Society, 1947
H, GILMAN, G C, GAINER
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A new approach to isoquinolines

Tetrahedron Letters, 1968
A, Hassner, R A, Arnold, R, Gault, A, Terada   +3 more
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Isoquinolines. 2. 3-(Dialkylaminoalkylamino)isoquinolines as potential antimalarial drugs

Journal of Medicinal Chemistry, 1970
J L, Neumeuer, K K, Weinhardt
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Isoquinoline derivatives

Chemistry of Heterocyclic Compounds, 1970
A. L. Mndzhoyan, �. A. Markaryan, T. M. Martirosyan   +2 more
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