(1) Synthesis of oligo(spiroketal)s from naturally occurring myo-inositol.
Sudo, A.; Sano, T.; Harada, M.; Ishida, D.
ACS Macro Lett. 2014, 3, 808 - 812. DOI: 10.1021/mz500353y
(2) Rigid triol and diol with adamantane-like core derived from naturally occurring myo-inositol and their polyaddition with diisocyanates.
Okamoto, S.; Onoue, S.; Kobayashi, M.; Sudo, A.
J. Polym. Sci. Part A: Polym. Chem. 2014, 52, 3498 - 3505. DOI: 10.1002/pola.27414
(3) Solid-state circularly polarised luminescence of atropisomeric fluorophores embedded in achiral myo-inositol-containing polyurethanes.
Amako, T.; Nakabayashi, K.; Sudo, A.; Fujiki, M.; Imai, Y.
Org. Biomol. Chem. 2015, 13, 2913 – 2917. DOI: 10.1039/C4OB02553A
(5) Metal-free reductive coupling of C=O and C=N bonds driven by visible light: use of perylene as a simple photoredox catalyst.
Okamoto, S.; Kojiyama, K.; Tsujioka, H.; Sudo, A.
Chem. Commun. 2016, 52, 11339 - 11342. (Back Cover Picture) DOI: 10.1039/C6CC05867A
(6) A Metal-Free Approach to 1,2-Diamines via Visible Light-Driven Reductive Coupling of Imines with Perylene as a Photoredox Catalyst.
Okamoto, S.; Ariki, R.; Tsujioka, H.; Sudo, A.
J. Org. Chem. 2017, 82, 9731-9736.
DOI: 10.1021/acs.joc.7b01838
(7) Organic Photoredox Catalyst with Substrate-capture Ability: A Perylene Derivative Bearing Urethane Moiety for Reductive Coupling of Ketones and Aldehydes under Visible Light.
Okamoto, S.; Tsujioka, H.; Sudo, A.
Chem. Lett. 2018, 47, 369-372. DOI:10.1246/cl.171160
