Works by Toshima, Kazunobu
Results: 79
Cover Feature: Designed Mannosylerythritol Lipid Analogues Exhibiting Both Selective Cytotoxicity Against Human Skin Cancer Cells and Recovery Effects on Damaged Skin Cells (Chem. Eur. J. 48/2024).
- Published in:
- Chemistry - A European Journal, 2024, v. 30, n. 48, p. 1, doi. 10.1002/chem.202484802
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- Article
Designed Mannosylerythritol Lipid Analogues Exhibiting Both Selective Cytotoxicity Against Human Skin Cancer Cells and Recovery Effects on Damaged Skin Cells.
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- Chemistry - A European Journal, 2024, v. 30, n. 48, p. 1, doi. 10.1002/chem.202401319
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Synthesis of Mannosylerythritol Lipid Analogues and their Self‐Assembling Properties, Recovery Effects on Damaged Skin Cells, and Antibacterial Activity.
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- Chemistry - A European Journal, 2022, v. 28, n. 55, p. 1, doi. 10.1002/chem.202201733
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- Article
Titelbild: Regioselective and Stereospecific β‐Arabinofuranosylation by Boron‐Mediated Aglycon Delivery (Angew. Chem. 46/2023).
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- Angewandte Chemie, 2023, v. 135, n. 46, p. 1, doi. 10.1002/ange.202313773
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Regioselective and Stereospecific β‐Arabinofuranosylation by Boron‐Mediated Aglycon Delivery.
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- Angewandte Chemie, 2023, v. 135, n. 46, p. 1, doi. 10.1002/ange.202307015
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Innenrücktitelbild: Synthesis of a Pentasaccharide Repeating Unit of Lipopolysaccharide Derived from Virulent E. coli O1 and Identification of a Glycotope Candidate of Avian Pathogenic E. coli O1 (Angew. Chem. 4/2021).
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- Angewandte Chemie, 2021, v. 133, n. 4, p. 2195, doi. 10.1002/ange.202015610
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Synthesis of a Pentasaccharide Repeating Unit of Lipopolysaccharide Derived from Virulent E. coli O1 and Identification of a Glycotope Candidate of Avian Pathogenic E. coli O1.
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- Angewandte Chemie, 2021, v. 133, n. 4, p. 1817, doi. 10.1002/ange.202013729
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Total Synthesis of Mannosylerythritol Lipids and Structure-Function Relationship Studies.
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- Journal of Oleo Science, 2024, v. 73, n. 4, p. 539, doi. 10.5650/jos.ess23222
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Enzyme-Catalyzed Preparation of Aliphatic Polythioester by Direct Polycondensation of Diacid Diester and Dithiol.
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- Macromolecular Rapid Communications, 2006, v. 27, n. 8, p. 605, doi. 10.1002/marc.200500836
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New Strategy for Enzymatic Synthesis of High-Molecular‐Weight Poly(butylene succinate) via Cyclic Oligomers.
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- Macromolecular Rapid Communications, 2006, v. 27, n. 3, p. 203, doi. 10.1002/marc.200500723
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Enzyme-Catalyzed Preparation of Aliphatic Polyesters Containing Thioester Linkages.
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- Macromolecular Rapid Communications, 2003, v. 24, n. 7, p. 467, doi. 10.1002/marc.200390070
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Organic Solvent-Free Enzymatic Transformation of Poly( ϵ-caprolactone) into Repolymerizable Oligomers in Supercritical Carbon Dioxide.
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- Macromolecular Rapid Communications, 2001, v. 22, n. 16, p. 1325, doi. 10.1002/1521-3927(20011101)22:16<1325::AID-MARC1325>3.0.CO;2-K
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Lipase-Catalyzed transformation of Poly(trimethylene carbonate) into Cyclic Monomer, Trimethylene Carbonate: A New Strategy for Sustainable Polymer Recycling Using an Enzyme.
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- Macromolecular Rapid Communications, 2001, v. 22, n. 3, p. 215, doi. 10.1002/1521-3927(200102)22:3<215::AID-MARC215>3.0.CO;2-#
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A new strategy for sustainable polymer recycling using an enzyme: poly(ε-caprolactone).
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- Macromolecular Rapid Communications, 2000, v. 21, n. 12, p. 860, doi. 10.1002/1521-3927(20000801)21:12<860::AID-MARC860>3.0.CO;2-U
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Enzyme-catalyzed polymerization of L-aspartate.
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- Macromolecular Rapid Communications, 1999, v. 20, n. 1, p. 7, doi. 10.1002/(SICI)1521-3927(19990101)20:1<7::AID-MARC7>3.0.CO;2-M
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Novel lipase-catalyzed ring-opening copolymerization of oxiranes and succinic anhydride forming polyesters bearing functional groups.
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- Macromolecular Rapid Communications, 1998, v. 19, n. 6, p. 295, doi. 10.1002/(SICI)1521-3927(19980601)19:6<295::AID-MARC295>3.0.CO;2-0
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Self‐Assembling Properties and Recovery Effects on Damaged Skin Cells of Chemically Synthesized Mannosylerythritol Lipids.
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- ChemBioChem, 2022, v. 23, n. 2, p. 1, doi. 10.1002/cbic.202100631
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Chemical approach for target-selective degradation of oligosaccharides using photoactivatable organic molecules.
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- Glycoconjugate Journal, 2015, v. 32, n. 7, p. 475, doi. 10.1007/s10719-015-9591-9
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Destabilization of vitelline membrane outer layer protein 1 homolog (VMO1) by C‐mannosylation.
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- FEBS Open Bio, 2023, v. 13, n. 3, p. 490, doi. 10.1002/2211-5463.13561
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Photodegradation of Target Oligosaccharides by Light-Activated Small Molecules.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 52, p. 10096, doi. 10.1002/anie.201005161
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Target-Selective Degradation of Oligosaccharides by a Light-Activated Small-Molecule-Lectin Hybrid.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 44, p. 8396, doi. 10.1002/anie.200702127
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2‐Phenylquinoline–Sugar Hybrids as Photoswitchable α‐Glucosidase Inhibitors.
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- Chemistry - An Asian Journal, 2019, v. 14, n. 9, p. 1409, doi. 10.1002/asia.201900203
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Target-Selective Fluorescence Imaging and Photocytotoxicity against H<sub>2</sub>O<sub>2</sub> High-Expressing Cancer Cells Using a Photoactivatable Theranostic Agent.
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- Chemistry - An Asian Journal, 2017, v. 12, n. 20, p. 2656, doi. 10.1002/asia.201701004
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Target-Selective Photodegradation of HIV-1 Protease and Inhibition of HIV-1 Replication in Living Cells by Designed Fullerene-Sugar Hybrids.
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- Chemistry - An Asian Journal, 2012, v. 7, n. 5, p. 911, doi. 10.1002/asia.201101043
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Degradation of Target Oligosaccharides by Anthraquinone-Lectin Hybrids with Light Switching.
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- Chemistry - An Asian Journal, 2012, v. 7, n. 1, p. 97, doi. 10.1002/asia.201100586
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Inhibition of Amyloid β Aggregation and Cytotoxicity by Photodegradation Using a Designed Fullerene Derivative.
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- Chemistry - An Asian Journal, 2011, v. 6, n. 9, p. 2312, doi. 10.1002/asia.201100421
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Photoinduced Glycosylation Using a Diarylthiophene as an Organo Lewis Photoacid Catalyst.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 20, p. 1, doi. 10.1002/ejoc.202300287
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Degradation of Poly(lactic acid) into Repolymerizable Oligomer using Montmorillonite K10 for Chemical Recycling.
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- Macromolecular Bioscience, 2005, v. 5, n. 9, p. 813, doi. 10.1002/mabi.200500086
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Enzymatic Transformation of Bacterial Polyhydroxyalkanoates into Repolymerizable Oligomers Directed towards Chemical Recycling.
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- Macromolecular Bioscience, 2005, v. 5, n. 7, p. 644, doi. 10.1002/mabi.200500030
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Synthesis and Chemical Recycling of Novel Poly(ester-urethane)s Using an Enzyme.
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- Macromolecular Bioscience, 2005, v. 5, n. 4, p. 277, doi. 10.1002/mabi.200400176
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Transformation of Biodegradable Polyesters into Cyclic Oligomers under Continuous Flow Using an Enzyme-Packed Column.
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- Macromolecular Bioscience, 2004, v. 4, n. 10, p. 936, doi. 10.1002/mabi.200400046
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Cover Picture: Macromol. Biosci. 10/2004.
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- Macromolecular Bioscience, 2004, v. 4, n. 10, p. 909, doi. 10.1002/mabi.200490022
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Enzymatic Synthesis and Chemical Recycling of Poly(carbonate-urethane).
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- Macromolecular Bioscience, 2004, v. 4, n. 8, p. 721, doi. 10.1002/mabi.200400042
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Lipase-Catalyzed Transformation of Poly(lactic acid) into Cyclic Oligomers.
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- Macromolecular Bioscience, 2004, v. 4, n. 3, p. 346, doi. 10.1002/mabi.200300094
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Enzymatic Synthesis and Polymerization of Cyclic Trimethylene Carbonate Monomer with/without Methyl Substituent.
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- Macromolecular Bioscience, 2003, v. 3, n. 8, p. 436, doi. 10.1002/mabi.200350013
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Enzymatic Ring-Opening Polymerization of Oxiranes and Dicarboxylic Anhydrides.
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- Macromolecular Bioscience, 2002, v. 2, n. 9, p. 429, doi. 10.1002/mabi.200290003
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Lipase-catalyzed selective transformation of polycaprolactone into cyclic dicaprolactone and its repolymerization in supercritical carbon dioxide.
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- Macromolecular Bioscience, 2002, v. 2, n. 6, p. 267, doi. 10.1002/1616-5195(200208)2:6<267::AID-MABI267>3.0.CO;2-F
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Lipase-Catalyzed Transformation of Unnatural-Type Poly(3-hydroxybutanoate) into Reactive Cyclic Oligomer.
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- Macromolecular Bioscience, 2002, v. 2, n. 2, p. 88, doi. 10.1002/1616-5195(20020201)2:2<88::AID-MABI88>3.0.CO;2-5
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Lipase-Catalyzed Ring-Opening Polymerization of β-Butyrolactone: End-Group Analysis of Poly(3-hydroxybutanoate) Using Supercritical Fluid Chromatography.
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- Macromolecular Bioscience, 2001, v. 1, n. 5, p. 171, doi. 10.1002/1616-5195(20010701)1:5<171::AID-MABI171>3.0.CO;2-5
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Lipase-catalyzed polymerization of diethyl carbonate and diol to aliphatic poly(alkylene carbonate).
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- Macromolecular Chemistry & Physics, 2000, v. 201, n. 14, p. 1632, doi. 10.1002/1521-3935(20000901)201:14<1632::AID-MACP1632>3.0.CO;2-P
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Perspectives for synthesis and production of polyurethanes and related polymers by enzymes directed toward green and sustainable chemistry.
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- Applied Microbiology & Biotechnology, 2006, v. 70, n. 1, p. 12, doi. 10.1007/s00253-005-0269-2
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Chemoenzymatic Synthesis and Chemical Recycling of Sustainable Polyurethanes.
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- ChemSusChem, 2008, v. 1, n. 1/2, p. 133, doi. 10.1002/cssc.200700055
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Cover Picture: Regioselective and Stereospecific β‐Arabinofuranosylation by Boron‐Mediated Aglycon Delivery (Angew. Chem. Int. Ed. 46/2023).
- Published in:
- Angewandte Chemie International Edition, 2023, v. 62, n. 46, p. 1, doi. 10.1002/anie.202313773
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- Publication type:
- Article
Regioselective and Stereospecific β‐Arabinofuranosylation by Boron‐Mediated Aglycon Delivery.
- Published in:
- Angewandte Chemie International Edition, 2023, v. 62, n. 46, p. 1, doi. 10.1002/anie.202307015
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Inside Back Cover: Synthesis of a Pentasaccharide Repeating Unit of Lipopolysaccharide Derived from Virulent E. coli O1 and Identification of a Glycotope Candidate of Avian Pathogenic E. coli O1 (Angew. Chem. Int. Ed. 4/2021).
- Published in:
- Angewandte Chemie International Edition, 2021, v. 60, n. 4, p. 2167, doi. 10.1002/anie.202015610
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- Publication type:
- Article
Synthesis of a Pentasaccharide Repeating Unit of Lipopolysaccharide Derived from Virulent E. coli O1 and Identification of a Glycotope Candidate of Avian Pathogenic E. coli O1.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 4, p. 1789, doi. 10.1002/anie.202013729
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- Article
Stereospecific β‐l‐Rhamnopyranosylation through an S<sub>N</sub>i‐Type Mechanism by Using Organoboron Reagents.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 42, p. 13858, doi. 10.1002/anie.201808045
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Improved total synthesis of incednam.
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- Journal of Antibiotics, 2013, v. 66, n. 3, p. 155, doi. 10.1038/ja.2013.4
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Builder performance in detergent formulations and biodegradability of partially dicarboxylated amylopectin.
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- Journal of the American Oil Chemists' Society (JAOCS), 1994, v. 71, n. 7, p. 749, doi. 10.1007/BF02541433
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Lipase-catalyzed ring-opening polymerization of lactide.
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- Macromolecular Rapid Communications, 1997, v. 18, n. 6, p. 477, doi. 10.1002/marc.1997.030180604
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