Substitution Effects of Alkene Dipeptide Isosteres on Adjacent Peptide Bond Rotation von Iio, Chihiro, Sato, Kohei, Mase, Nobuyuki, Narumi, Tetsuo

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Hydrazide-Mediated Solubilizing Strategy for Poorly Soluble Peptides Using a Dialkoxybenzaldehyde Linker von Tanaka, Shoko, Narumi, Tetsuo, Mase, Nobuyuki, Sato, Kohei

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Microwave-Assisted Synthesis of Azacoumarin Fluorophores and the Fluorescence Characterization von Takano, Hikaru, Narumi, Tetsuo, Nomura, Wataru, Tamamura, Hirokazu

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Amide-to-chloroalkene substitution for overcoming intramolecular acyl transfer challenges in hexapeptidic neuromedin U receptor 2 agonists von Narumi, Tetsuo, Toyama, Daichi, Fujimoto, Junko, Kyan, Ryuji, Sato, Kohei, Mori, Kenji, Pearson, James T, Mase, Nobuyuki, Takayama, Kentaro

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Remote Stereoinduction in the Organocuprate-Mediated Allylic Alkylation of Allylic gem-Dichlorides: Highly Diastereoselective Synthesis of (Z)‑Chloroalkene Dipeptide Isosteres von Kobayakawa, Takuya, Narumi, Tetsuo, Tamamura, Hirokazu

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Late-Stage Derivatization of Oleanolic Acid-Based Anti-HIV-1 Compounds von Takeuchi, Reon, Fujimoto, Junko, Taguchi, Yoshinori, Ide, Ryuji, Kyan, Ryuji, Sato, Kohei, Mase, Nobuyuki, Yokoyama, Masaru, Harada, Shigeyoshi, Narumi, Tetsuo

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Late-Stage Solubilization of Poorly Soluble Peptides Using Hydrazide Chemistry von Sato, Kohei, Tanaka, Shoko, Wang, Junzhen, Ishikawa, Kenya, Tsuda, Shugo, Narumi, Tetsuo, Yoshiya, Taku, Mase, Nobuyuki

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Tuning the Catalyst Reactivity of Imidazolylidene Catalysts through Substituent Effects on the N‑Aryl Groups von Kyan, Ryuji, Sato, Kohei, Mase, Nobuyuki, Watanabe, Naoharu, Narumi, Tetsuo

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7‑Hydroxy‑N‑Methylquinolinium Chromophore: A Photolabile Protecting Group for Blue-Light Uncaging von Narumi, Tetsuo, Miyata, Koichi, Nii, Akitaka, Sato, Kohei, Mase, Nobuyuki, Furuta, Toshiaki

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Chemoselective Umpolung of Enals for Asymmetric Homoenolate Cross-Annulation of Enals and Aldehydes Catalyzed by N‑Heterocyclic Carbene von Ide, Ryuji, Kyan, Ryuji, Phuc Le, Thien, Kitagawa, Yuya, Sato, Kohei, Mase, Nobuyuki, Narumi, Tetsuo

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Utilization of the Heavy Atom Effect for the Development of a Photosensitive 8‑Azacoumarin-Type Photolabile Protecting Group von Takano, Hikaru, Narumi, Tetsuo, Nomura, Wataru, Furuta, Toshiaki, Tamamura, Hirokazu

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Flexibility of small molecular CD4 mimics as HIV entry inhibitors von Kobayakawa, Takuya, Ohashi, Nami, Hirota, Yuki, Takahashi, Kohei, Yamada, Yuko, Narumi, Tetsuo, Yoshimura, Kazuhisa, Matsushita, Shuzo, Harada, Shigeyoshi, Tamamura, Hirokazu

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Design, synthesis and biological evaluation of low molecular weight CXCR4 ligands von Sakyiamah, Maxwell M., Kobayakawa, Takuya, Fujino, Masayuki, Konno, Makoto, Narumi, Tetsuo, Tanaka, Tomohiro, Nomura, Wataru, Yamamoto, Naoki, Murakami, Tsutomu, Tamamura, Hirokazu

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Isostere-Based Design of 8‑Azacoumarin-Type Photolabile Protecting Groups: A Hydrophilicity-Increasing Strategy for Coumarin-4-ylmethyls von Narumi, Tetsuo, Takano, Hikaru, Ohashi, Nami, Suzuki, Akinobu, Furuta, Toshiaki, Tamamura, Hirokazu

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Development of the 8-aza-3-bromo-7-hydroxycoumarin-4-ylmethyl group as a new entry of photolabile protecting groups von Takano, Hikaru, Narumi, Tetsuo, Ohashi, Nami, Suzuki, Akinobu, Furuta, Toshiaki, Nomura, Wataru, Tamamura, Hirokazu

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Stereoselective Formation of Trisubstituted (Z)‑Chloroalkenes Adjacent to a Tertiary Carbon Stereogenic Center by Organocuprate-Mediated Reduction/Alkylation von Narumi, Tetsuo, Kobayakawa, Takuya, Aikawa, Haruo, Seike, Shunsuke, Tamamura, Hirokazu

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A minimally cytotoxic CD4 mimic as an HIV entry inhibitor von Mizuguchi, Takaaki, Harada, Shigeyoshi, Miura, Tomoyuki, Ohashi, Nami, Narumi, Tetsuo, Mori, Hiromi, Irahara, Yu, Yamada, Yuko, Nomura, Wataru, Matsushita, Shuzo, Yoshimura, Kazuhisa, Tamamura, Hirokazu

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Synthesis of a self-assembling gold nanoparticle-supported organocatalyst for enamine-based asymmetric aldol reactions von Sóti, Péter Lajos, Yamashita, Hiroki, Sato, Kohei, Narumi, Tetsuo, Toda, Mitsuo, Watanabe, Naoharu, Marosi, György, Mase, Nobuyuki

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CD4 mimics as HIV entry inhibitors: Lead optimization studies of the aromatic substituents von Narumi, Tetsuo, Arai, Hiroshi, Yoshimura, Kazuhisa, Harada, Shigeyoshi, Hirota, Yuki, Ohashi, Nami, Hashimoto, Chie, Nomura, Wataru, Matsushita, Shuzo, Tamamura, Hirokazu

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CD4 mimics targeting the mechanism of HIV entry von Yamada, Yuko, Ochiai, Chihiro, Yoshimura, Kazuhisa, Tanaka, Tomohiro, Ohashi, Nami, Narumi, Tetsuo, Nomura, Wataru, Harada, Shigeyoshi, Matsushita, Shuzo, Tamamura, Hirokazu

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