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[文献書誌] Akira Otaka et al.: "SmI_2-Mediated Reduction of γ,γ-Difluoro-α,β-enoates with Application to the Synthesis of Functionalized (Z)-Fluoroalkene Type Dipeptide Isosteres"J.Org.Chem.. 69. 1634-1645 (2004)
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[文献書誌] Akira Otaka et al.: "Synthesis of fluorine-containing Bioisosteres corresponding to phosphoamino acids and dipeptide units"Biopolymers. 76. 140-149 (2004)
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[文献書誌] Nobutaka Fujii et al.: "Molecular-size Reduction of a Potent CXCR4-chemokine Antagonist Using Orthogonal Combination of Conformation- and Sequence-based Libraries"Angew.Chem., Int.Ed.. 42. 3251-3253 (2003)
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[文献書誌] Akira Otaka et al.: "Application of Samarium Diiodide (SmI_2)-induced Reduction of γ-Acetoxy-α,β-enoates with α-Specific Kinetic Electrophilic Trapping for the Synthesis of Amino Acid Derivatives"Chem.Commun.. 1834-1835 (2003)
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[文献書誌] Hirokazu Tamamura et al.: "Synthesis of Potent CXCR4 Inhibitors Possessing Low Cytotoxicity and Improved Biostability Based on T140 Derivatives"Org.Biomol.Chem.. 1. 3656-3662 (2003)
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[文献書誌] Hirokazu Tamamura et al.: "Enhancement of the T140-based Pharmacophores Leads to the Development of More Potent and Bio-stable CXCR4 Antagonists"Org.Biomol.Chem.. 1. 3663-3669 (2003)
