Search Results - "Suginome, H."

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    Dimerization of anilines and benzylamines with mercury(II) oxide-iodine reagent by Orito, Kazuhiko, Hatakeyama, Takahiro, Takeo, Mitsuhiro, Uchiito, Shiho, Tokuda, Masao, Suginome, Hiroshi

    Published in Tetrahedron (16-07-1998)
    “…By treatment with mercury(II) oxide-iodine reagent in dichloromethane at room temperature, substituted anilines were transformed to the corresponding…”
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    Regioselective synthesis of β,γ-unsaturated acids by the electrochemical carboxylation of allylic bromides using a reactive-metal anode by Tokuda, Masao, Kabuki, Takashi, Katoh, Yoshitaka, Suginome, Hiroshi

    Published in Tetrahedron letters (08-05-1995)
    “…Electrolysis of γ-mono and disubstituted allylic bromides in the presence of atmospheric pressure of carbon dioxide using a platinum cathode and a magnesium…”
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    Tandem cyclization of N-allylaminyl radicals: Stereoselective synthesis of 1,2,5-trisubstituted pyrrolizidines by Senboku, Hisanori, Kajizuka, Yoshinori, Hasegawa, Hikaru, Fujita, Hirotake, Suginome, Hiroshi, Orito, Kazuhiko, Tokuda, Masao

    Published in Tetrahedron (21-05-1999)
    “…Radical reaction of N-allylalk-4-enylaminyl radicals, generated from the corresponding N-chloroamines by treatment with Bu 3SnH-AIBN in refluxing toluene, was…”
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    Studies on carboxylation of alkoxy-substituted benzyl alcohols via direct lithiation and bromine-lithium exchange: Synthesis of phthalides and phthalideisoquinoline alkaloids by Orito, Kazuhiko, Miyazawa, Mamoru, Suginome, Hiroshi

    Published in Tetrahedron (27-02-1995)
    “…Conversion of alkoxy-substituted benzyl alcohols to the corresponding phthalides by carboxylation via ortho lithiation and bromine-lithium exchange was…”
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    Transformation of epiandrosterone into 3-oxa-, 3-thia-, 3-selena-, and 3-aza-17-oxaandrostanes of the 5 alpha series based on beta-scission of alkoxyl radicals by Suginome, H, Wang, J B

    Published in Steroids (01-08-1990)
    “…3 beta-Hydroxy-5 alpha-androstan-17-one was transformed into 17-oxa-5 alpha-androstan-3 beta-ol in five steps involving conversion of the 17-ketone via the…”
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