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Langmuir : the ACS Journal of Surfaces and Colloids|July 6, 2017
Water-Proton Relaxivities of Radical Nanoparticles Self-Assembled via Hydration or Dehydration ProcessesKosuke Morishita, Yuna Okamoto, Shuhei Murayama, et al.
Organic Letters|February 24, 2021
β-Glycosyl Trifluoroborates as Precursors for Direct α-C-Glycosylation: Synthesis of 2-Deoxy-α-C-glycosidesDaiki Takeda, Makoto Yoritate, Hiroki Yasutomi, et al.
Bioorganic & Medicinal Chemistry Letters|May 6, 2004
Design, synthesis, and structure-activity relationship of new isobenzofuranone ligands of protein kinase CYoshiyasu Baba, Yosuke Ogoshi, Go Hirai, et al.
Bioorganic & Medicinal Chemistry Letters|May 6, 2004
Evaluation of series of isobenzofuranone dimers as PKCalpha ligands: implication for the distance between the two ligand binding sitesYoshiyasu Baba, Satoshi Mayumi, Go Hirai, et al.
Israel Journal of Chemistry|June 30, 2017
Synthesis of the Right-Side Structure of Type B PhysalinsMasaki Morita, Shuntaro Kojima, Megumi Ohkubo, et al.
Organic Letters|March 28, 2013
Unexpected Diels-Alder/carbonyl-ene cascade toward the biomimetic synthesis of chloropupukeananinTakahiro Suzuki, Yuria Miyajima, Kaname Suzuki, et al.
Bioorganic & Medicinal Chemistry|April 8, 2014
RE12 derivatives displaying Vaccinia H1-related phosphatase (VHR) inhibition in the presence of detergent and their anti-proliferative activity against HeLa cellsFrédéric Thuaud, Shuntaro Kojima, Go Hirai, et al.
Organic & Biomolecular Chemistry|November 23, 2016
Total synthesis of natural derivatives and artificial analogs of 13-oxyingenol and their biological evaluationTakayuki Ohyoshi, Yuki Tamura, Ichiro Hayakawa, et al.
Glycoconjugate Journal|March 20, 2023
Synthesis and biological activity of ganglioside GM3 analogues with a (S)-CHF-Sialoside linkage and an alkyne tagEisuke Ota, Daiki Takeda, Kana Oonuma, et al.
Chemistry, an Asian Journal|October 31, 2025
Linkage-Editing of 6,6'-Diacyl Neotrehalose and Evaluation of Mincle Activation AbilityRintaro Nakahashi, Hiroaki Matoba, Yuki Sakai, et al.
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