Hatsuo Ishida - Publications

Affiliations: 
Case Western Reserve University, Cleveland Heights, OH, United States 
Area:
Polymer Chemistry, Plastics Technology

37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Iguchi D, Ohashi S, Abarro GJE, Yin X, Winroth S, Scott C, Gleydura M, Jin L, Kanagasegar N, Lo C, Arza CR, Froimowicz P, Ishida H. Development of Hydrogen-Rich Benzoxazine Resins with Low Polymerization Temperature for Space Radiation Shielding. Acs Omega. 3: 11569-11581. PMID 31459257 DOI: 10.1021/acsomega.8b01297  0.6
2017 Han L, Iguchi D, Gil PS, Heyl T, Sedwick VM, Arza CR, Ohashi S, Lacks DJ, Ishida H. Oxazine Ring-Related Vibrational Modes of Benzoxazine Monomers Using Fully Aromatically Substituted, Deuterated, (15)N Isotope Exchanged and Oxazine-Ring-Substituted Compounds and Theoretical Calculation. The Journal of Physical Chemistry. A. PMID 28747051 DOI: 10.1021/acs.jpca.7b05249  0.6
2016 Froimowicz P, R Arza C, Han L, Ishida H. Smart, Sustainable, and Ecofriendly Chemical Design of Fully Bio-Based Thermally Stable Thermosets Based on Benzoxazine Chemistry. Chemsuschem. PMID 27480785 DOI: 10.1002/cssc.201600577  0.6
2016 Makyio H, Shimabukuro J, Suzuki T, Imamura A, Ishida H, Kiso M, Ando H, Kato R. Six independent fucose-binding sites in the crystal structure of Aspergillus oryzae lectin. Biochemical and Biophysical Research Communications. PMID 27318092 DOI: 10.1016/j.bbrc.2016.06.069  0.36
2016 Kobayashi D, Ueki A, Yamaji T, Nagao K, Imamura A, Ando H, Kiso M, Ishida H. Efficient Synthesis of the Lewis A Tandem Repeat. Molecules (Basel, Switzerland). 21. PMID 27187324 DOI: 10.3390/molecules21050614  0.36
2016 Goto K, Sawa M, Tamai H, Imamura A, Ando H, Ishida H, Kiso M. The Total Synthesis of Starfish Ganglioside GP3 Bearing a Unique Sialyl Glycan Architecture. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27172064 DOI: 10.1002/chem.201600970  0.36
2016 Sriwilaijaroen N, Sadagopan M, Imamura A, Ando H, Ishida H, Sakai M, Ishitsubo E, Hori T, Moriya S, Ishikawa T, Kuwata K, Odagiri T, Tashiro M, Hiramatsu H, Tsukamoto K, et al. A Novel Potent and Highly Specific Inhibitor against Influenza Viral N1-N9 Neuraminidases: Insight into Neuraminidase-inhibitor Interactions. Journal of Medicinal Chemistry. PMID 27095056 DOI: 10.1021/acs.jmedchem.5b01863  0.36
2016 Komura N, Suzuki KG, Ando H, Konishi M, Koikeda M, Imamura A, Chadda R, Fujiwara TK, Tsuboi H, Sheng R, Cho W, Furukawa K, Furukawa K, Yamauchi Y, Ishida H, et al. Raft-based interactions of gangliosides with a GPI-anchored receptor. Nature Chemical Biology. PMID 27043189 DOI: 10.1038/nchembio.2059  0.36
2016 Tanase M, Imamura A, Ando H, Ishida H, Kiso M. A 5-Ureido-Modified Sialyl Donor: A Tool for the Synthesis of α-Sialosides. Organic Letters. PMID 26938981 DOI: 10.1021/acs.orglett.6b00403  0.36
2016 Froimowicz P, Zhang K, Ishida H. Intramolecular Hydrogen Bonding in Benzoxazines: When Structural Design Becomes Functional. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26797690 DOI: 10.1002/chem.201503477  0.6
2016 Arza CR, Froimowicz P, Ishida H. Triggering effect caused by elemental sulfur as a mean to reduce the polymerization temperature of benzoxazine monomers Rsc Advances. 6: 35144-35151. DOI: 10.1039/c6ra04420d  0.6
2016 Ohashi S, Pandey V, Arza CR, Froimowicz P, Ishida H. Simple and low energy consuming synthesis of cyanate ester functional naphthoxazines and their properties Polymer Chemistry. 7: 2245-2252. DOI: 10.1039/c5py01854d  0.6
2016 Alhwaige AA, Herbert MM, Alhassan SM, Ishida H, Qutubuddin S, Schiraldi DA. Laponite/multigraphene hybrid-reinforced poly(vinyl alcohol) aerogels Polymer (United Kingdom). 91: 180-186. DOI: 10.1016/j.polymer.2016.03.077  0.6
2016 Wan Hassan WA, Liu J, Howlin BJ, Ishida H, Hamerton I. Examining the influence of bisphenol A on the polymerisation and network properties of an aromatic benzoxazine Polymer (United Kingdom). 88: 52-62. DOI: 10.1016/j.polymer.2016.01.041  0.6
2016 Froimowicz P, Rodriguez Arza C, Ohashi S, Ishida H. Tailor-made and chemically designed synthesis of coumarin-containing benzoxazines and their reactivity study toward their thermosets Journal of Polymer Science, Part a: Polymer Chemistry. 54: 1428-1435. DOI: 10.1002/pola.27994  0.6
2016 Froimowicz P, R. Arza C, Han L, Ishida H. Cover Picture: Smart, Sustainable, and Ecofriendly Chemical Design of Fully Bio-Based Thermally Stable Thermosets Based on Benzoxazine Chemistry (ChemSusChem 15/2016) Chemsuschem. 9: 1898. DOI: 10.1002/cssc.201600967  0.6
2015 Yamagishi M, Hosoda-Yabe R, Tamai H, Konishi M, Imamura A, Ishida H, Yabe T, Ando H, Kiso M. Structure-Activity Relationship Study of the Neuritogenic Potential of the Glycan of Starfish Ganglioside LLG-3 (‡). Marine Drugs. 13: 7250-74. PMID 26690179 DOI: 10.3390/md13127062  0.36
2015 Thubsuang U, Ishida H, Wongkasemjit S, Chaisuwan T. Advanced and economical ambient drying method for controlled mesopore polybenzoxazine-based carbon xerogels: Effects of non-ionic and cationic surfactant on porous structure. Journal of Colloid and Interface Science. 459: 241-9. PMID 26298286 DOI: 10.1016/j.jcis.2015.08.022  0.76
2015 Liu X, Yanagawa T, Leopold DA, Chang C, Ishida H, Fujii N, Duyn JH. Arousal transitions in sleep, wakefulness, and anesthesia are characterized by an orderly sequence of cortical events. Neuroimage. 116: 222-31. PMID 25865143 DOI: 10.1016/j.neuroimage.2015.04.003  0.32
2015 Zhang K, Ishida H. An anomalous trade-off effect on the properties of smart ortho-functional benzoxazines Polymer Chemistry. 6: 2541-2550. DOI: 10.1039/c5py00031a  0.6
2015 Ohashi S, Kilbane J, Heyl T, Ishida H. Synthesis and Characterization of Cyanate Ester Functional Benzoxazine and Its Polymer Macromolecules. 48: 8412-8417. DOI: 10.1021/acs.macromol.5b02285  0.6
2015 Zhang K, Ishida H. Thermally stable polybenzoxazines via ortho-norbornene functional benzoxazine monomers: Unique advantages in monomer synthesis, processing and polymer properties Polymer (United Kingdom). 66: 240-248. DOI: 10.1016/j.polymer.2015.04.044  0.6
2015 Zhang K, Liu J, Ohashi S, Liu X, Han Z, Ishida H. Synthesis of high thermal stability polybenzoxazoles via ortho-imide-functional benzoxazine monomers Journal of Polymer Science, Part a: Polymer Chemistry. 53: 1330-1338. DOI: 10.1002/pola.27565  0.6
2015 Tamai H, Imamura A, Ogawa J, Ando H, Ishida H, Kiso M. First Total Synthesis of Ganglioside GAA-7 from Starfish Asterias amurensis versi-color European Journal of Organic Chemistry. DOI: 10.1002/ejoc.201500606  0.36
2014 Mahfud R, Lacks D, Ishida H, Qutubuddin S. Molecular dynamic simulations of self-assembly of amphiphilic comb-like anionic polybenzoxazines. Langmuir : the Acs Journal of Surfaces and Colloids. 30: 11858-65. PMID 25222627 DOI: 10.1021/la501466z  0.6
2013 Mahfud R, Agag T, Ishida H, Shaikh S, Qutubuddin S. Synthesis and evaluation of novel anionic polymeric surfactants based on polybenzoxazines. Journal of Colloid and Interface Science. 407: 339-47. PMID 23890593 DOI: 10.1016/j.jcis.2013.06.042  0.6
2013 Alhwaige AA, Agag T, Ishida H, Qutubuddin S. Biobased chitosan/polybenzoxazine cross-linked films: preparation in aqueous media and synergistic improvements in thermal and mechanical properties. Biomacromolecules. 14: 1806-15. PMID 23631553 DOI: 10.1021/bm4002014  0.6
2009 Nakai R, Iida S, Takahashi T, Tsujita T, Okamoto S, Takada C, Akasaka K, Ichikawa S, Ishida H, Kusaka H, Akinaga S, Murakata C, Honda S, Nitta M, Saya H, et al. K858, a novel inhibitor of mitotic kinesin Eg5 and antitumor agent, induces cell death in cancer cells. Cancer Research. 69: 3901-9. PMID 19351824 DOI: 10.1158/0008-5472.CAN-08-4373  0.36
2008 Komori T, Ando T, Imamura A, Li YT, Ishida H, Kiso M. Design and efficient synthesis of novel GM2 analogues with respect to the elucidation of the function of GM2 activator. Glycoconjugate Journal. 25: 647-61. PMID 18368480 DOI: 10.1007/s10719-008-9117-9  0.36
2008 Li YT, Li SC, Kiso M, Ishida H, Mauri L, Raimondi L, Bernardi A, Sonnino S. Effect of structural modifications of ganglioside GM2 on intra-molecular carbohydrate-to-carbohydrate interaction and enzymatic susceptibility. Biochimica Et Biophysica Acta. 1780: 353-61. PMID 17967427 DOI: 10.1016/j.bbagen.2007.09.019  0.36
2006 Fuse T, Ando H, Imamura A, Sawada N, Ishida H, Kiso M, Ando T, Li SC, Li YT. Synthesis and enzymatic susceptibility of a series of novel GM2 analogs. Glycoconjugate Journal. 23: 329-43. PMID 16897176 DOI: 10.1007/s10719-006-5704-9  0.36
2003 Li YT, Li SC, Ishida H, Kiso M, Raimondi L, Bernardi A, Sonnino S. Structural basis for the enzymatic resistance of the GM2 ganglioside. Methods in Enzymology. 363: 242-64. PMID 14579580 DOI: 10.1016/S0076-6879(03)01056-5  0.36
2003 Goward GR, Sebastiani D, Schnell I, Spiess HW, Kim HD, Ishida H. Benzoxazine oligomers: evidence for a helical structure from solid-state NMR spectroscopy and DFT-based dynamics and chemical shift calculations. Journal of the American Chemical Society. 125: 5792-800. PMID 12733920 DOI: 10.1021/ja029059r  0.6
1999 Sonnino S, Brocca P, Acquotti D, Bernardi A, Raimondi L, Kiso M, Ishida H, Li SC, Li YT. The structural basis for the susceptibility of gangliosides to enzymatic degradation. Bioscience Reports. 19: 163-8. PMID 10513893  0.36
1999 Li YT, Li SC, Hasegawa A, Ishida H, Kiso M, Bernardi A, Brocca P, Raimondi L, Sonnino S. Structural basis for the resistance of Tay-Sachs ganglioside GM2 to enzymatic degradation. The Journal of Biological Chemistry. 274: 10014-8. PMID 10187778  0.36
1997 Ishida H, Ito Y, Tanahashi E, Li YT, Kiso M, Hasegawa A. Synthesis of 6'-GM2, a regioisomer of ganglioside GM2, for studying the mechanism of action of GM2 activator. Carbohydrate Research. 302: 223-7. PMID 9291574  0.36
1988 Kojima T, Hasegawa T, Ishida H, Fujita M, Okamoto S. Griseofulvin-induced photodermatitis--report of six cases. The Journal of Dermatology. 15: 76-82. PMID 2969014  0.36
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