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Representative Publications
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Ko, M.-S.; Roh, T.-H.; Desale, P. P.; Choi, S.-U.; Cho, D.-G. Effectsof Electron-Withdrawingand Electron-DonatingGroupsonAromaticityin CyclicConjugatedPolyenes J. Am. Chem. Soc. 2024, 146, 6266-6273
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Ko, M.-S.; Hong, J.-H.; Desale, P. P.; Roh, T.-H.; Cho, D.-G. Fundamental difference between simple arenes and PAHs found in o-PAH-connected porphyrins Org. Chem. Front. 2023, 10, 5644-5650
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Ko, M.-S.; Hong, J.-H.; Aslam, A.S.; Lee, Y.; Cho, D.-G. Synthesis of Dioxa-1,7-naphthicorrole and Its Oxidized Porphyrinoid as a Potential Built-In Linker for Biomolecules J. Org. Chem. 2023, 88, 722-726
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Ko, M.-S.; Hong, J.-H.; Aslam, A.S.; Rao, P.Sankara; Desale, P. P.; Choi, J.; Lee, Y.; Cho, D.-G. o-(2-Thienyl)vinylarene as an Alternative Synthetic Motif for Porphyrinoids: o-Arene-Connected Porphyrinoids Org. Lett. 2022, 24, 8812-8815
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Hong, J.-H.; Aslam, A.S.; Cho, B.; Ko, M.-S.; Kim, Y.; Heo, J.; Cho, D.-G. Carbaporphyrin Dimers That Bear a Rigid Naphthalene Motif as an Internal Strap Org. Lett. 2021, 23, 1846-1850
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Aslam, A.S.; Fuwad, A.; Ryu, H.; Selvaraj, B.; Song, J.-W; Kim, D.W.; Kim, S.M.; Lee, J.W.; Jeon, T.-J.; Cho, D.-G. Synthetic Anion Transporters as Endoplasmic Reticulum (ER) Stress Inducers Org. Lett. 2019, 21, 7828-7832
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Ko, M.-S.; Aslam, A.S.; Cho, D.-G. Cooperative ion pair receptor based on tolan as a Li+/HSO4- selective extractor and fluorescent indicator Tetrahedron Lett. 2018, 59, 4475-4478
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Hong, J.-H.; Aslam, A.S.; Ko, M.-S.; Choi, J; Lee, Y; Cho, D.-G. Bond Rotation in an Aromatic Carbaporphyrin: Allyliporphyrin Chem. Eur. J. 2018, 24, 10054-10058
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Aslam, A.S.; Hong, J.-H.; Shin, J.-H.; Cho, D.-G. Synthesis of a Phlorin from a Meso-Fused Anthriporphyrin by a Diels–Alder Strategy Angew. Chem. Int. Ed. 2017, 56, 16247-16251
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Shin, J.-H.; Hong, J.-H.; Ko, M.-S.; Cho, D.-G. Fluorescent and cooperative ion pair receptor based on tolan for Na+ (or Li+) and HSO4−: logic AND gate Chem. Commun. 2017, 53, 11414-11417
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Hong, J.-H.; Kurapati, S.; Jo, Y.-H.; Shin, J.-H.; Cho, D.-G. Accelerated hydration reaction of an unsymmetrical tolan evidenced by a Hg(II)-trapped macrocycle and its application as a Hg(II)-selective indicator Chem. Commun. 2016, 52, 10759-10762
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Hong, J.-H.; Aslam, A.S.; Ishida, M.; Mori, S.; Furuta, H.; Cho, D.-G. 2-(Naphthalen-1-yl)thiophene as a New Motif for Porphyrinoids: Meso-Fused Carbaporphyrin J. Am. Chem. Soc. 2016, 138, 4992-4995
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Hong, J.-H.; Atta, A.K.; Jung, K.-B.; Kim, S.-B.; Heo, J.-S.; Cho, D.-G. Conformationally Locked Tolans, β‑Sheet Structures, and Photophysical Properties Org. Lett. 2015, 17, 6222-6225
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Lee, E.-B.; Ryu, H.-I.; Lee, I.-S.; Choi, S.-B.; Hong, J.-H.; Kim, S.-M.; Jeon, T.-J.; Cho, D.-G. Synthetic anion transporters that bear a terminal ethynyl group Chem. Commun. 2015, 51, 9339-9342
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Jo, Y.-H.; Chidalla, N.; Cho, D.-G. Bis-ureidoquinoline as a Selective Fluoride Anion Sensor through Hydrogen-Bond Interactions. J. Org. Chem. 2014, 9418–9422
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Atta, A. K.; Kim, S.-B.; Heo, J.-S.; Cho, D.-G. Hg(II)-mediated intramolecular cyclization reaction in aqueous media and its application as Hg(II) selective indicator. Org. lett. 2013, 1072-1075
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Kim, S.-B.; Cho, D.-G. Hg(II)-Selective Fluorescent Indicator: One-Step Synthesis. Eur. J. Org. Chem. 2012, 2495-2498
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Jung, K.-B.; Kim, S. K.; Lynch, V. M.; Cho, D.-G.; Sessler, J. L. A calix[2]phenol[2]pyrrole and a fused pyrrolidine-containing derivative. Chem. Commun. 2012, 48, 2495-2497.
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Kim, S. K.; Gross, D. E.; Cho, D.-G.; Lynch, V. M.; Sessler, J. L. N-Tosylpyrrolidine Calix[4]pyrrole: Synthesis and Ion Binding Studies. J. Org. Chem. 2011, 76, 1005-1012.
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Cho, S.; Yoon, Z.-S.; Kim, K. S.; Yoon, M.-C.; Cho, D.-G.; Sessler, J. L.; Kim, D. Defining Spectroscopic Features of Heteroannulenic Antiaromatic Porphyrinoids. J. Phys. Chem. Lett. 2010, 1, 895-900.
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Cho, D.-G.; Sessler, J. L. Mordern Reaction-Based Indicator Systems. Chem. Soc. Rev. 2009, 38, 1647-1662.
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Cho, D-G.; Kim J. H.; Sessler, J. L. The Benzil-Cyanide Reaction and Its Application to the Development of a Selective Cyanide Anion Indicator. J. Am. Chem. Soc. 2008, 130, 12163-12167.
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Sessler, J. L.; Cho, D.-G. The Benzil Rearrangement Reaction: Trapping of a Hitherto Minor Product and Its Application to the Development of a Selective Cyanide Anion Indicator. Org. Lett. 2008, 10, 73-75.
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Yoon, Z. S.; Cho, D.-G.; Kim, K. S.; Sessler, J. L.; Kim, D. Nonlinear optical properties as a guide to aromaticity in congeneric pentapyrrolic expanded porphyrins: Pentaphyrin, sapphyrin, isosmaragdyrin, and orangarin. J. Am. Chem. Soc. 2008, 130, 6930–6931.
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Cho, D-G.; Plitt, P.; Kim, S. K.; Lynch, V.; Hong, S.-J.; Lee, C.-H.; Sessler, J. L. Dioxabenzosapphyrin: A New Benzodifuran-Derived Sapphyrin Analogue. J. Am. Chem. Soc. 2008, 130, 10502–10503.
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Boul, P. J.; Cho, D.-G.; Aminur Rahman, G. M.; Marquez, M.; Ou, Z.; Kadish, K. M.; Guldi, D. M.; Sessler, J. L. Sapphyrin-Nanotube Assemblies. J. Am. Chem. Soc. 2007, 129, 5683–5687.
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Sessler, J. L.; Cho, D.-G.; Lynch, V. Diindolylquinoxalines: Effective Indole-Based Receptors for Phosphate Anion. J. Am. Chem. Soc. 2006 ,128, 16518-16519.
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Sessler, J. L.; Cho, D.-G.; Stepien, M.; Lynch, V.; Waluk, J.; Yoon, Z. S.; Kim, D. Inverted Sapphyrin: Inverted Sapphyrin: a New Family of Doubly N-Confused Expanded Porphyrins. J. Am. Chem. Soc. 2006, 128, 12640-12641.
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