Enantioselective Total Synthesis of (+)-Ophiobolin A von Tsuna, Kazuhiro, Noguchi, Naoyoshi, Nakada, Masahisa

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Design and Identification of a GPR40 Full Agonist (SCO-267) Possessing a 2‑Carbamoylphenyl Piperidine Moiety von Furukawa, Hideki, Miyamoto, Yasufumi, Hirata, Yasuhiro, Watanabe, Koji, Hitomi, Yuko, Yoshitomi, Yayoi, Aida, Jumpei, Noguchi, Naoyoshi, Takakura, Nobuyuki, Takami, Kazuaki, Miwatashi, Seiji, Hirozane, Yoshihiko, Hamada, Teruki, Ito, Ryo, Ookawara, Mitsugi, Moritoh, Yusuke, Watanabe, Masanori, Maekawa, Tsuyoshi

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Research on the pig liver esterase (PLE)-catalyzed kinetic resolution of half-esters derived from prochiral diesters von Noguchi, Naoyoshi, Tsuna, Kazuhiro, Nakada, Masahisa

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Synthetic Studies on (+)-Ophiobolin A:  Asymmetric Synthesis of the Spirocyclic CD-Ring Moiety von Noguchi, Naoyoshi, Nakada, Masahisa

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Synthesis of medium-sized carbocyclic ketones via the intramolecular B-alkyl Liebeskind–Srogl coupling reaction von Tsuna, Kazuhiro, Noguchi, Naoyoshi, Nakada, Masahisa

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Convergent Total Synthesis of (+)-Ophiobolin A von Tsuna, Kazuhiro, Noguchi, Naoyoshi, Nakada, Masahisa

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Preparation of a new chiral building block containing a benzylic quaternary stereogenic center and a formal total synthesis of (−)-physostigmine von Asakawa, Kaori, Noguchi, Naoyoshi, Takashima, Shingo, Nakada, Masahisa

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Convergent Total Synthesis of (+)‐Ophiobolin A von Tsuna, Kazuhiro, Noguchi, Naoyoshi, Nakada, Masahisa

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Inhibition of 3-phosphoglycerate dehydrogenase (PHGDH) by indole amides abrogates de novo serine synthesis in cancer cells von Mullarky, Edouard, Xu, Jiayi, Robin, Anita D., Huggins, David J., Jennings, Andy, Noguchi, Naoyoshi, Olland, Andrea, Lakshminarasimhan, Damodharan, Miller, Michael, Tomita, Daisuke, Michino, Mayako, Su, Taojunfeng, Zhang, Guoan, Stamford, Andrew W., Meinke, Peter T., Kargman, Stacia, Cantley, Lewis C.

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Discovery of a novel series of indolinylpyrimidine-based GPR119 agonists: Elimination of ether-a-go-go-related gene liability using a hydrogen bond acceptor-focused approach von Kamaura, Masahiro, Kubo, Osamu, Sugimoto, Hiromichi, Noguchi, Naoyoshi, Miyashita, Hirohisa, Abe, Shinichi, Matsuda, Kae, Tsujihata, Yoshiyuki, Odani, Tomoyuki, Iwasaki, Shinji, Murata, Toshiki, Sato, Kenjiro

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Enantioselective Total Synthesis of (+)-OphiobolinA von Tsuna, Kazuhiro, Noguchi, Naoyoshi, Nakada, Masahisa

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Discovery of 3,5-Diphenyl-4-methyl-1,3-oxazolidin-2-ones as Novel, Potent, and Orally Available Δ‑5 Desaturase (D5D) Inhibitors von Fujimoto, Jun, Okamoto, Rei, Noguchi, Naoyoshi, Hara, Ryoma, Masada, Shinichi, Kawamoto, Tetsuji, Nagase, Hiroki, Tamura, Yumiko Okano, Imanishi, Mitsuaki, Takagahara, Shuichi, Kubo, Kazuki, Tohyama, Kimio, Iida, Koichi, Andou, Tomohiro, Miyahisa, Ikuo, Matsui, Junji, Hayashi, Ryouta, Maekawa, Tsuyoshi, Matsunaga, Nobuyuki

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Convergent Total Synthesis of (+)-OphiobolinA von Tsuna, Kazuhiro, Noguchi, Naoyoshi, Nakada, Masahisa

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Convergent Total Synthesis of (+)-Ophiobolin A von Tsuna, Kazuhiro, Noguchi, Naoyoshi, Nakada, Masahisa

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Convergent Total Synthesis of (+)‐Ophiobolin A von Tsuna, Kazuhiro, Noguchi, Naoyoshi, Nakada, Masahisa

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Gram-scale preparation of the antibiotic lead compound salicyl-AMS, a potent inhibitor of bacterial salicylate adenylation enzymes von Kinarivala, Nihar, Standke, Lisa C, Guney, Tezcan, Ji, Cheng, Noguchi, Naoyoshi, Asano, Yasutomi, Tan, Derek S

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Convergent Total Synthesis of (+)-OphiobolinA von Tsuna, Kazuhiro, Noguchi, Naoyoshi, Nakada, Masahisa

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Convergent Total Synthesis of (+)‐Ophiobolin A von Tsuna, Kazuhiro, Noguchi, Naoyoshi, Nakada, Masahisa

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Macrocyclic compound and use thereof von NIIDA, Ayumu, IKOMA, Minoru, FUKUSHI, Hideto, MATSUMOTO, Shigemitsu, NOGUCHI, Naoyoshi, SASAKI, Satoshi, MAEKAWA, Tsuyoshi, KOBAYASHI, Toshitake, HARA, Ryoma

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Macrocyclic compound and use thereof von Maekawa, Tsuyoshi, Matsumoto, Shigemitsu, Noguchi, Naoyoshi, Ikoma, Minoru, Hara, Ryoma, Niida, Ayumu, Fukushi, Hideto, Sasaki, Satoshi, Kobayashi, Toshitake

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