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Jose A Lopez - One of the best experts on this subject based on the ideXlab platform.

Yongsun Park - One of the best experts on this subject based on the ideXlab platform.

  • Regioselective catalytic hydrogenation of nitrogen rings of fused heteroaromatic Compounds with an iridium-triphenylphosphine complex
    Catalysis Letters, 1995
    Co-Authors: Chong Shik Chin, Yongsun Park
    Abstract:

    Catalytic hydrogenation of fused heteroaromatic Compounds, acridine, quinoline and quinaldine, selectively occurs at the nitrogen containing rings to give 9,10-dihydroacridine, 1,2,3,4-tetrahydroquinoline and 1,2,3,4-tetrahydroquinaldine in the homogeneous solution prepared from the reaction of [Ir(COD)(PPh_3)(PhCN)]ClO_4 (COD=1,5-cyclooctadiene) with H_2 (5 atm) at 50°C, while isoquinoline and indole are not hydrogenated under the same experimental conditions. In the presence of the Rhodium analog [Rh(COD)(PPh_3)(PhCN)]ClO_4 however, both isoquinoline and indole are also hydrogenated at the nitrogen containing rings, which is understood in terms of heterogeneous catalysis by metallic Rhodium powders produced in the reduction of the Rhodium Compound under the same experimental conditions (50°C, 5 atm of H_2).

Cristina Tejel - One of the best experts on this subject based on the ideXlab platform.

Michael B. Hursthouse - One of the best experts on this subject based on the ideXlab platform.

Chong Shik Chin - One of the best experts on this subject based on the ideXlab platform.

  • Regioselective catalytic hydrogenation of nitrogen rings of fused heteroaromatic Compounds with an iridium-triphenylphosphine complex
    Catalysis Letters, 1995
    Co-Authors: Chong Shik Chin, Yongsun Park
    Abstract:

    Catalytic hydrogenation of fused heteroaromatic Compounds, acridine, quinoline and quinaldine, selectively occurs at the nitrogen containing rings to give 9,10-dihydroacridine, 1,2,3,4-tetrahydroquinoline and 1,2,3,4-tetrahydroquinaldine in the homogeneous solution prepared from the reaction of [Ir(COD)(PPh_3)(PhCN)]ClO_4 (COD=1,5-cyclooctadiene) with H_2 (5 atm) at 50°C, while isoquinoline and indole are not hydrogenated under the same experimental conditions. In the presence of the Rhodium analog [Rh(COD)(PPh_3)(PhCN)]ClO_4 however, both isoquinoline and indole are also hydrogenated at the nitrogen containing rings, which is understood in terms of heterogeneous catalysis by metallic Rhodium powders produced in the reduction of the Rhodium Compound under the same experimental conditions (50°C, 5 atm of H_2).