Search Results - "Ogo, Takashi"

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  1. 1

    Direct Carbonylation at a C−H Bond in the Benzene Ring of 2-Phenyloxazolines Catalyzed by Ru3(CO)12. Scope, Limitations, and Mechanistic Aspects by Ie, Yutaka, Chatani, Naoto, Ogo, Takashi, Marshall, Daniel R, Fukuyama, Takahide, Kakiuchi, Fumitoshi, Murai, Shinji

    Published in Journal of organic chemistry (10-03-2000)
    “…The ruthenium-catalyzed carbonylation at a C−H bond in the benzene ring of a 2-phenyloxazoline is described. The reaction of 2-phenyloxazolines with CO and…”
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    Journal Article
  2. 2

    Practical Synthesis of Chiral 3‑(Hydroxyiminomethyl)adipic Acid, a Key Intermediate of the ROR‑γ Inhibitor JTE-151, via Crystallization-Induced Dynamic Resolution by Takiguchi, Hiromu, Watanabe, Takashi, Ogo, Takashi, Ishibashi, Hideaki, Yokota, Katsuyuki, Obika, Shingo, Inaba, Takashi

    Published in Organic process research & development (15-12-2023)
    “…A practical six-step process for the production of chiral 3-(hydroxyiminomethyl)­adipic acid 4 featuring highly efficient crystallization-induced dynamic…”
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    Journal Article
  3. 3

    One-Step Synthesis of Heteroaromatic-Fused Pyrrolidines via Cyclopropane Ring-Opening Reaction:  Application to the PKCβ Inhibitor JTT-010 by Tanaka, Masahiro, Ubukata, Minoru, Matsuo, Takafumi, Yasue, Katsutaka, Matsumoto, Katsuya, Kajimoto, Yasuyuki, Ogo, Takashi, Inaba, Takashi

    Published in Organic letters (16-08-2007)
    “…A ring-opening reaction of cyclopropanes with five-membered heteroaromatics having a leaving group at C(2) was found to provide heteroaromatic-fused…”
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    Journal Article
  4. 4

    One-step synthesis of heteroaromatic-fused pyrrolidines via cyclopropane ring-opening reaction: application to the PKCbeta inhibitor JTT-010 by Tanaka, Masahiro, Ubukata, Minoru, Matsuo, Takafumi, Yasue, Katsutaka, Matsumoto, Katsuya, Kajimoto, Yasuyuki, Ogo, Takashi, Inaba, Takashi

    Published in Organic letters (16-08-2007)
    “…A ring-opening reaction of cyclopropanes with five-membered heteroaromatics having a leaving group at C(2) was found to provide heteroaromatic-fused…”
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    Journal Article
  5. 5