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The Journal of Organic Chemistry|April 20, 2021
Stereoselective Synthesis of the Southern Hemisphere Acyclic Domain of Neaumycin BHiroya Takeshita, Tomoya Sugai, Haruhiko Fuwa
The Journal of Organic Chemistry|March 26, 2021
Cobalt-Catalyzed Hartung-Mukaiyama Cyclization of γ-Hydroxy Olefins: Stereocontrolled Synthesis of the Tetrahydrofuran Moiety of Amphidinolide NMasaki Ohta, Shota Kato, Tomoya Sugai, et al.
The Journal of Organic Chemistry|April 16, 2021
Ruthenium-Catalyzed Intramolecular Double Hydrofunctionalization of Alkynes. Synthesis of Spirocyclic Hemiaminal Ethers and Their Lewis Acid-Mediated Cleavage/Nucleophilic AdditionKazuma Nishimura, Ryohei Hanzawa, Tomoya Sugai, et al.
Acta Crystallographica. Section E, Crystallographic Communications|August 5, 2017
Crystal structure of (-)-methyl (<i>R</i>,<i>E</i>)-4-[(2<i>R</i>,4<i>R</i>)-2-amino-2-tri-chloro-methyl-1,3-dioxolan-4-yl]-4-hy-droxy-2-methyl-but-2-enoateTakeshi Oishi, Mayu Kidena, Tomoya Sugai, et al.
Acta Crystallographica. Section E, Crystallographic Communications|June 17, 2016
Crystal structure of (+)-N-[(1R,5S,6S,9S)-5-hydroxy-methyl-3,3,9-trimethyl-8-oxo-2,4,7-trioxabi-cyclo-[4.3.0]nonan-9-yl]acetamideTakeshi Oishi, Shun Tsuzaki, Tomoya Sugai, et al.
Chemical Science|June 24, 2021
Total synthesis and complete configurational assignment of amphirionin-2Shota Kato, Daichi Mizukami, Tomoya Sugai, et al.
The Journal of Organic Chemistry|October 3, 2025
Odorless and Air-Stable Thionating Reagent for Broad Scope Thioamide Synthesis without H<sub>2</sub>S EmissionTomoya Sugai, Mizuki Oyanagi, Takashi Nakamura, et al.
Bioorganic & Medicinal Chemistry Letters|January 16, 2024
Design and synthesis of unique morphinan-type molecules: Their application to the search for the unexplored binding domain between opioid receptors and morphinan ligandsKenta Maeda, Tomoya Sugai, Akihisa Tokuda, et al.
Acta Crystallographica. Section E, Crystallographic Communications|February 24, 2015
Crystal structure of (±)-(4RS,5RS,7SR)-4-[(1RS,2RS,3RS,6RS)-3-benzo-yloxy-2-(2-hy-droxy-ethyl)-6-meth-oxy-meth-oxy-2-methyl-cyclo-hex-yl]-8,10,10-trimethyl-2-oxo-1,3-dioxa-spiro-[4.5]dec-8-en-7-yl benzoate benzene monosolvateTakeshi Oishi, Yuu Yamaguchi, Keisuke Fukaya, et al.
Acta Crystallographica. Section E, Crystallographic Communications|May 22, 2015
Crystal structure of (±)-(1SR,5SR,6SR,7SR,10SR,11SR,13SR)-13-benz-yloxy-7-meth-oxy-meth-oxy-11,15,18,18-tetra-methyl-3-oxo-2,4-dioxa-tetra-cyclo-[12.3.1.0(1,5).0(6,11)]octa-deca-14,16-dien-10-yl benzoateTakeshi Oishi, Keisuke Fukaya, Yu Yamaguchi, et al.
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