M. Arisawa

发表

Three-dimensional structure-activity relationship study of belactosin A and its stereo- and regioisomers: development of potent proteasome inhibitors by a stereochemical diversity-oriented strategy.

S. Shuto, A. Matsuda, H. Yokosawa, 2009, Organic & biomolecular chemistry.

Cyclopropane-based stereochemical diversity-oriented conformational restriction strategy: histamine H3 and/or H4 receptor ligands with the 2,3-methanobutane backbone.

T. Hirokawa, S. Shuto, S. Yamada, 2012, Organic & biomolecular chemistry.

Investigation of the bioactive conformation of histamine H3 receptor antagonists by the cyclopropylic strain-based conformational restriction strategy.

T. Hirokawa, S. Shuto, S. Yamada, 2010, Journal of medicinal chemistry.

Characterization of Imidazopyridine Compounds as Negative Allosteric Modulators of Proton-Sensing GPR4 in Extracellular Acidification-Induced Responses

S. Shuto, D. Im, T. Nakakura, 2015, PloS one.

Development of isomerization and cycloisomerization with use of a ruthenium hydride with N-heterocyclic carbene and its application to the synthesis of heterocycles.

A. Nishida, M. Arisawa, Kazuyuki Takahashi, 2006, The Journal of organic chemistry.

Ligand-free Suzuki–Miyaura coupling using ruthenium(0) nanoparticles and a continuously irradiating microwave system

Y. Tamenori, T. Honma, M. Arisawa, 2017 .

Self‐Assembled Multilayer‐Stabilized Nickel Nanoparticle Catalyst for Ligand‐Free Cross‐Coupling Reactions: in situ Metal Nanoparticle and Nanospace Simultaneous Organization

S. Shuto, Y. Tamenori, T. Honma, 2016 .

The Actual Active Species of Sulfur-Modified Gold-Supported Palladium as a Highly Effective Palladium Reservoir in the Suzuki–Miyaura Coupling

S. Shuto, M. Arisawa, Naoyuki Hoshiya, 2011 .

Development of an Enyne Metathesis/Isomerization/Diels-Alder One-Pot Reaction for the Synthesis of a Novel Near-Infrared (NIR) Dye Core.

H. Aoyama, Y. Fujii, T. Uno, 2015, Chemistry.

Redox Switching of Orthoquinone-Containing Aromatic Compounds with Hydrogen and Oxygen Gas.

H. Ishikawa, M. Arisawa, Masaki Matsuda, 2016, Angewandte Chemie.

DJ-1 cooperates with PYCR1 in cell protection against oxidative stress.

S. Shuto, T. Niki, H. Ariga, 2013, Biochemical and biophysical research communications.

First Asymmetric Total Synthesis and Insight into the Structure of Laurenidificin

Tetsuya Kobayashi, M. Arisawa, Michinori Sumimoto, 2017 .

Development of environmentally benign organometallic catalysis for drug discovery and its application.

M. Arisawa, 2007, Chemical & pharmaceutical bulletin.

[Development of environmentally friendly organometallic catalysis for drug discovery and its application to heterocyclic chemistry].

M. Arisawa, 2007, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.

Development of a Method for Preparing a Highly Reactive and Stable, Recyclable and Environmentally Benign Organopalladium Catalyst Supported on Sulfur‐Terminated Gallium Arsenide(001): A Three‐Component Catalyst, {Pd}‐S‐GaAs(001), and its Properties

Y. Arakawa, M. Shimoda, S. Tsukamoto, 2006 .

Novel Palladium Catalyst Supported on GaAs(001) Passivated by Ammonium Sulfide

Y. Arakawa, M. Shimoda, S. Tsukamoto, 2004 .

Synthesis of 5''-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent: The first antagonists modified at the N1-ribose moiety.

S. Shuto, A. Matsuda, T. Murayama, 2008, Bioorganic & medicinal chemistry letters.

Iridium-Catalyzed Isomerization/Cycloisomerization/Aromatization of N-Allyl-N-sulfonyl-o-(λ1-silylethynyl)aniline Derivatives to Give Substituted Indole Derivatives.

M. Arisawa, Kenichi Murai, M. Sako, 2021, Organic letters.

Ni-Catalyzed Cycloisomerization between 3-Phenoxy Acrylic Acid Derivatives and Alkynes via Intramolecular Cleavage and Formation of the C-O Bond To Give 2,3-Disubstituted Benzofurans.

J. Hasegawa, H. Aoyama, M. Arisawa, 2019, Organic letters.

Design and Synthesis of Cyclopropane Congeners of Resolvin E2, an Endogenous Proresolving Lipid Mediator, as Its Stable Equivalents.

S. Shuto, T. Matsuda, H. Fukuda, 2016, Organic letters.

Synthesis of a series of 3,4-methanoarginines as side-chain conformationally restricted analogues of arginine.

S. Shuto, R. Silverman, K. Yamaguchi, 2011, Bioorganic & medicinal chemistry.

Formation of self-assembled multi-layer stable palladium nanoparticles for ligand-free coupling reactions

T. Miyazaki, S. Arai, S. Shuto, 2015 .

Ligand‐Free Buchwald–Hartwig Aromatic Aminations of Aryl Halides Catalyzed by Low‐Leaching and Highly Recyclable Sulfur‐Modified Gold‐Supported Palladium Material

S. Shuto, M. Al-Amin, T. Honma, 2012 .

Preparation of Tethered Palladium Catalysis Supported on Gold(111) and Its Surface Characterization by X-ray Photoelectron Spectroscopy (XPS)

S. Shuto, M. Shimoda, S. Tsukamoto, 2008 .

Sulfur modification of Au via treatment with Piranha solution provides low-Pd releasing and recyclable Pd material, SAPd.

S. Shuto, M. Shimoda, Y. Yamashita, 2010, Journal of the American Chemical Society.

Palladium Material Supported on GaAs(001) or Gold for Drug Development

S. Shuto, M. Arisawa, Naoyuki Hoshiya, 2010 .

Metal-Free Nitrogen-Containing Polyheterocyclic Near-Infrared (NIR) Absorption Dyes: Synthesis, Absorption Properties, and Theoretical Calculation of Substituted 5-Methylisoindolo[2,1-a]quinolines

T. Takagi, N. Kawashita, Y. Fujii, 2019, ACS omega.

Pd-Catalyzed Migratory Cycloisomerization of N-Allyl- o-allenylaniline Derivatives.

H. Aoyama, M. Arisawa, H. Fujioka, 2019, Organic letters.

Design and Synthesis of 1,2-Deoxy-pyranose Derivatives of Spliceostatin A toward Prostate Cancer Treatment.

Y. Kaneda, Keisuke Nimura, M. Arisawa, 2020, ACS medicinal chemistry letters.

Chemoselective Transformations of Aromatic Methoxymethyl Ethers Using Trialkylsilyl Triflate and 2,2′-Bipyridyl

M. Arisawa, H. Fujioka, Kenichi Murai, 2019, ACS omega.

Preparation of Nitrogen-Containing Heterocycles Using Ring-Closing Metathesis (RCM) and Its Application to Natural Product Synthesis

A. Nishida, M. Arisawa, M. Nakagawa, 2006 .

Nickel Nanoparticle-catalyzed Carboxylation of Unsaturated Hydrocarbon with CO2 Using Sulfur-modified Au-supported Nickel Material

S. Shuto, M. Arisawa, Nozomi Saito, 2019, Chemistry Letters.

Preparation of chiral bromomethylenecyclopropane and its use in Suzuki-Miyaura coupling: synthesis of the arylmethyl-(Z)-cyclopropane structure core.

S. Shuto, H. Fukuda, M. Tanabe, 2013, The Journal of organic chemistry.

Reusable Immobilized Iron(II) Nanoparticle Precatalysts for Ligand-Free Kumada Coupling

Y. Tamenori, K. Tsuruta, T. Honma, 2018, ACS Applied Nano Materials.

Synthesis of 8-Substituted Analogues of Cyclic ADP-4-Thioribose and Their Unexpected Identification as Ca2+-Mobilizing Full Agonists.

S. Shuto, T. Kameda, H. Fukuda, 2017, Journal of medicinal chemistry.

Design, Synthesis, and Chemical and Biological Properties of Cyclic ADP-4-Thioribose as a Stable Equivalent of Cyclic ADP-Ribose.

T. Hirokawa, S. Shuto, B. Potter, 2014, Messenger.

A fluorescence-based method for evaluating inositol 1,4,5-trisphosphate receptor ligands: determination of subtype selectivity and partial agonist effects.

S. Shuto, M. Arisawa, A. Tanimura, 2013, Journal of biotechnology.

Development of a new class of proteasome inhibitors with an epoxyketone warhead: Rational hybridization of non-peptidic belactosin derivatives and peptide epoxyketones.

S. Shuto, A. Asai, Y. Unno, 2014, Bioorganic & medicinal chemistry.

Investigation of the noncovalent binding mode of covalent proteasome inhibitors around the transition state by combined use of cyclopropylic strain-based conformational restriction and computational modeling.

T. Hirokawa, S. Shuto, T. Kameda, 2013, Journal of medicinal chemistry.

Identification of a Potent and Selective GPR4 Antagonist as a Drug Lead for the Treatment of Myocardial Infarction.

S. Shuto, H. Fukuda, H. Kurose, 2016, ACS medicinal chemistry letters.

Design and synthesis of a phenyl C-glycoside derivative of Spliceostatin A and its biological evaluation toward prostate cancer treatment

Y. Kaneda, Keisuke Nimura, M. Arisawa, 2019 .

Nonmetathesis Heterocycle Formation by Ruthenium-Catalyzed Intramolecular [2 + 2] Cycloaddition of Allenamide-enes to Azabicyclo[3.1.1]heptanes

S. Shuto, Takashi Matsumoto, M. Arisawa, 2016 .

One‐Pot Ring‐Closing Metathesis (RCM)/Oxidation by an Assisted Tandem Ruthenium Catalysis for the Synthesis of 2‐Quinolones

S. Shuto, M. Arisawa, H. Kato, 2011 .

Non-metathesis reactions of ruthenium carbene catalysts and their application to the synthesis of nitrogen-containing heterocycles.

A. Nishida, M. Arisawa, Kazuyuki Takahashi, 2007, Chemical record.

Development of novel reactions using ruthenium carbene catalyst and its application to novel methods for preparing nitrogen-containing heterocycles

A. Nishida, M. Arisawa, Kazuyuki Takahashi, 2005 .

Development of a Recyclable and Low‐Leaching Palladium Catalyst Supported on Sulfur‐Modified Gallium Arsenide (001) for Use in Suzuki–Miyaura Coupling

S. Shuto, H. Yoshikawa, M. Shimoda, 2009 .

Palladium-nanoparticle-catalyzed 1,7-palladium migration involving C-H activation, followed by intramolecular amination: regioselective synthesis of N1-arylbenzotriazoles and an evaluation of their inhibitory activity toward indoleamine 2,3-dioxygenase.

S. Shuto, H. Sugimoto, J. Wouters, 2014, The Journal of organic chemistry.

Aromatic Enamide/Ene Metathesis toward Substituted Indoles and Its Application to the Synthesis of Indomethacins

S. Shuto, A. Nishida, M. Arisawa, 2009 .

Oxidative Biaryl Coupling Reaction of Phenol Ether Derivatives Using a Hypervalent Iodine(III) Reagent

Y. Kita, M. Arisawa, R. Hamada, 1998 .

Hypervalent Iodine(III)-Induced Intramolecular Cyclization of α-(Aryl)alkyl-β-dicarbonyl Compounds: A Convenient Synthesis of Benzannulated and Spirobenzannulated Compounds

Y. Kita, M. Arisawa, N. Ramesh, 2001 .

Efficient oxidative biaryl coupling reaction of phenol ether derivatives using hypervalent iodine(III) reagents

Y. Kita, M. Arisawa, S. Takizawa, 2001 .

An intriguing effect of Yb(OTf)3-TMSCl in the halogenation of 1,1-disubstituted alkenes by NXS: selective synthesis of allyl halides

A. Nishida, M. Arisawa, M. Nakagawa, 2002 .

Design, Synthesis, and Identification of 4″α-Azidoethyl-cyclic ADP-Carbocyclic-ribose as a Highly Potent Analogue of Cyclic ADP-Ribose, a Ca(2+)-Mobilizing Second Messenger.

S. Shuto, T. Kameda, H. Fukuda, 2016, Journal of medicinal chemistry.

Synthesis of 7-Deaza-cyclic Adenosine-5'-diphosphate-carbocyclic-ribose and Its 7-Bromo Derivative as Intracellular Ca(2+)-Mobilizing Agents.

S. Shuto, H. Fukuda, T. Murayama, 2015, The Journal of organic chemistry.

Design and Synthesis of Cyclic ADP-4-Thioribose as a Stable Equivalent of Cyclic ADP-Ribose, a Calcium Ion-Mobilizing Second Messenger**

T. Hirokawa, S. Shuto, B. Potter, 2013, Angewandte Chemie.

Design and synthesis of 4″,6″-unsaturated cyclic ADP-carbocyclic-ribose, a Ca2+-mobilizing agent selectively active in T cells

S. Shuto, A. Matsuda, B. Potter, 2008 .

Ruthenium-Catalyzed 1,6-Aromatic Enamide-Silylalkyne Cycloisomerization: Approach to 2,3-Disubstituted Indoles.

M. Arisawa, H. Fujioka, Shohei Ohno, 2017, The Journal of organic chemistry.

Cycloisomerization between Aryl Enol Ether and Silylalkynes under Ruthenium Hydride Catalysis: Synthesis of 2,3-Disubstituted Benzofurans.

M. Arisawa, H. Fujioka, Shohei Ohno, 2017, Organic letters.

One‐Pot Olefin Isomerization/Aliphatic Enamine Ring‐Closing Metathesis/Oxidation/1,3‐Dipolar Cycloaddition for the Synthesis of Isoindolo[1,2‐a]isoquinolines

S. Shuto, Y. Fujii, M. Arisawa, 2015 .

One-pot ring-closing metathesis/1,3-dipolar cycloaddition through assisted tandem ruthenium catalysis: synthesis of a dye with isoindolo[2,1-a]quinoline structure.

S. Shuto, Yoshihiro Ito, Mika Ito, 2013, Angewandte Chemie.

Ruthenium‐Catalyzed Cycloisomerization and Its Application to the Synthesis of (±)‐Cinchonaminone

S. Shuto, Koujirou Yamamoto, M. Arisawa, 2012 .

Safe Removal of the Allyl Protecting Groups of Allyl Esters using a Recyclable, Low-Leaching and Ligand-Free Palladium Nanoparticle Catalyst

S. Shuto, A. Otaka, H. Fukuda, 2015 .

Pd/TiO2-Photocatalyzed Self-Condensation of Primary Amines To Afford Secondary Amines at Ambient Temperature.

M. Arisawa, Kensuke Kobayashi, S. Saito, 2018, Organic letters.

Self-Assembled Multilayer Iron(0) Nanoparticle Catalyst for Ligand-Free Carbon-Carbon/Carbon-Nitrogen Bond-Forming Reactions.

K. Harada, Y. Tamenori, K. Tsuruta, 2020, Organic letters.

Entry to Chiral 1,1,2,3-Tetrasubstituted Arylcyclopropanes by Pd(II)-Catalyzed Arylation via Directing Group-Mediated C(sp3)-H Activation.

S. Shuto, H. Fukuda, M. Arisawa, 2017, The Journal of organic chemistry.

Palladium-catalyzed arylation of cyclopropanes via directing group-mediated C(sp3)-H bond activation to construct quaternary carbon centers: synthesis of cis- and trans-1,1,2-trisubstituted chiral cyclopropanes.

S. Shuto, M. Arisawa, Takaaki Kobayashi, 2013, Organic letters.

A novel synthesis of substituted quinolines using ring-closing metathesis (RCM): its application to the synthesis of key intermediates for anti-malarial agents

A. Nishida, M. Arisawa, M. Nakagawa, 2004 .

Palladium Nanoparticle‐Catalyzed Direct Ethynylation of Aliphatic Carboxylic Acid Derivatives via C(sp3)H Bond Functionalization

S. Shuto, M. Al-Amin, N. Chatani, 2014 .

Synthesis of Chiral Bicyclic Lactams Using Ring Closure Metathesis: Synthesis of (-)-Coniceine and (S)-Pyrrolam A

A. Nishida, M. Arisawa, M. Mori, 1997 .

Design and synthesis of the stabilized analogs of belactosin A with the unnatural cis-cyclopropane structure.

S. Shuto, A. Asai, Y. Unno, 2013, Organic & biomolecular chemistry.

Selective isomerization of a terminal olefin catalyzed by a ruthenium complex: the synthesis of indoles through ring-closing metathesis.

A. Nishida, M. Arisawa, M. Nakagawa, 2002, Angewandte Chemie.

Development of isomerization and cycloisomerization with use of a ruthenium hydride with N-heterocyclic carbene and its application to the synthesis of heterocycles.

A. Nishida, M. Arisawa, Kazuyuki Takahashi, 2006, The Journal of organic chemistry.

Indomethacin Analogues that Enhance Doxorubicin Cytotoxicity in Multidrug Resistant Cells without Cox Inhibitory Activity.

S. Shuto, Yoshihiro Ito, Mika Ito, 2011, ACS medicinal chemistry letters.

Absorption, Fluorescence, and Two-Photon Excitation Ability of 5-Phenylisolidolo[2,1-a]quinolines

T. Nemoto, Y. Tsutsumi, T. Takagi, 2020, ACS omega.

Construction of chiral 1,2-cycloalkanopyrrolidines from L-proline using ring closing metathesis (RCM).

A. Nishida, M. Arisawa, M. Nakagawa, 2000, Chemical & pharmaceutical bulletin.

Total synthesis of (+)-(S)-angustureine and the determination of the absolute configuration of the natural product angustureine

A. Nishida, M. Arisawa, M. Nakagawa, 2005 .

Synthesis of substituted 1,2-dihydroquinolines and quinolines using ene–ene metathesis and ene–enol ether metathesis

A. Nishida, M. Arisawa, M. Nakagawa, 2001 .

Concise synthesis of azacycloundecenes using ring-closing metathesis (RCM)

A. Nishida, M. Arisawa, M. Nakagawa, 2000 .

Alantrypinone and its derivatives: synthesis and antagonist activity toward insect GABA receptors.

A. Nishida, Takayuki Watanabe, M. Arisawa, 2009, Bioorganic & medicinal chemistry.

Suzuki–Miyaura cross-coupling reactions using a low-leaching and highly recyclable gold-supported palladium material and two types of microwave equipments

S. Shuto, M. Al-Amin, M. Arisawa, 2013 .

Recent Development of Ring Closing Metathesis Approach to Bioactive Heterocycles: Synthesis of Nakadomarin A, Quinolines, and Indoles

A. Nishida, M. Arisawa, M. Nakagawa, 2009 .

Practical synthesis of a 3, 4, 4a, 5, 8, 8a-hexahydro-2H-isoquinoline-1, 6-dione ring system by the Diels-Alder reaction of an optically active dienophile, a 5, 6-dihydro-1H-pyridin-2-one derivative, with siloxydiene

A. Nishida, M. Arisawa, M. Nakagawa, 2003 .

Oxidative Intramolecular Phenolic Coupling Reaction Induced by a Hypervalent Iodine(III) Reagent: Leading to Galanthamine-Type Amaryllidaceae Alkaloids

Y. Kita, M. Arisawa, R. Hamada, 1998 .

Stereoselective Construction of 2,7-Disubstituted fused-Bis Tetrahydrofuran Skeletons: Biomimetic-Type Synthesis and Biological Evaluation of (±)- and (-)-Aplysiallene and Their Derivatives.

Kuniaki Suzuki, M. Arisawa, H. Fujioka, 2015, The Journal of organic chemistry.

Double carbonylation of aryl iodides with amines under an atmospheric pressure of carbon monoxide using sulfur-modified Au-supported palladium

S. Shuto, M. Arisawa, Nozomi Saito, 2015 .

Synthesis of 2,3- and 3,4-methanoamino acid equivalents with stereochemical diversity and their conversion into the tripeptide proteasome inhibitor belactosin a and its highly potent cis-cyclopropane stereoisomer.

S. Shuto, A. Matsuda, H. Yokosawa, 2008, Organic letters.

Concise synthesis of oxacyclic compounds using highly discriminative two-way transformations of α,β-unsaturated esters in the presence of enones.

H. Aoyama, M. Arisawa, H. Fujioka, 2017, Chemical communications.

Structurally novel highly potent proteasome inhibitors created by the structure-based hybridization of nonpeptidic belactosin derivatives and peptide boronates.

S. Shuto, A. Asai, Y. Unno, 2014, Journal of medicinal chemistry.

Thermal [2 + 2]-cycloaddition between silylalkynes and allenylphenols followed by the nucleophilic addition of water: metal-free and economical synthesis of arylcyclobutenals

H. Aoyama, M. Arisawa, H. Fujioka, 2020 .

Nickel-Catalyzed Suzuki–Miyaura Coupling of a Tertiary Iodocyclopropane with Wide Boronic Acid Substrate Scope: Coupling Reaction Outcome Depends on Radical Species Stability

S. Shuto, H. Fukuda, H. Abe, 2015 .

Development of second generation gold-supported palladium material with low-leaching and recyclable characteristics in aromatic amination.

S. Arai, S. Shuto, Takatoshi Sato, 2013, The Journal of organic chemistry.

Ring-opening 1,3-arylboration of arylcyclopropanes mediated by BCl3

M. Arisawa, Kenichi Murai, Yui Kuboki, 2020, RSC advances.

An Unexpected Intermolecular Chiral Biaryl Coupling Reaction Induced by a Hypervalent Iodine(III) Reagent: Synthesis of Potential Precursor for Ellagitannin.

Y. Kita, M. Arisawa, N. Ramesh, 1999 .

An unexpected intermolecular chiral biaryl coupling reaction induced by a hypervalent iodine(III) reagent: synthesis of potential precursor for ellagitannin

Y. Kita, M. Arisawa, N. Ramesh, 1999 .

Design, Synthesis, and Monoamine Oxidase Inhibitory Activity of (+)-Cinchonaminone and Its Simplified Derivatives.

S. Shuto, H. Aoyama, M. Arisawa, 2021, ACS medicinal chemistry letters.

Absorption, fluorescence, and two-photon excitation ability of 5-phenyl-13-arylisoindolo[2,1-a]quinolines prepared by one-pot reaction of ring-closing metathesis and 1,3-dipolar cycloaddition

T. Nemoto, K. Jang, Y. Fujii, 2023, Dyes and Pigments.

Development of a Sulfur-Modified Glass-Supported Pd Nanoparticle Catalyst for Suzuki-Miyaura Coupling.

S. Shuto, Y. Tamenori, T. Honma, 2016, Chemical & pharmaceutical bulletin.

Safe Removal of the Allyl Protecting Groups of Allyl Esters Using a Recyclable, Low‐Leaching and Ligand‐Free Palladium Nanoparticle Catalyst.

S. Shuto, A. Otaka, H. Fukuda, 2015 .

Ligand-free Suzuki-Miyaura coupling with sulfur-modified gold-supported palladium in the synthesis of a conformationally-restricted cyclopropane compound library with three-dimensional diversity.

S. Shuto, Y. Kogami, Takatoshi Sato, 2014, ACS combinatorial science.

Cyclopropane-based conformational restriction of GABA by a stereochemical diversity-oriented strategy: identification of an efficient lead for potent inhibitors of GABA transports.

S. Shuto, S. Yamada, E. Masuda, 2013, Bioorganic & medicinal chemistry.

Non-Directed β- or γ-C(sp3)–H Functionalization of Saturated Nitrogen-Containing Heterocycles

M. Arisawa, M. Miyoshi, Kenichi Murai, 2021 .

Cycloisomerization promoted by the combination of a ruthenium-carbene catalyst and trimethylsilyl vinyl ether, and its application in the synthesis of heterocyclic compounds: 3-methylene-2,3-dihydroindoles and 3-methylene-2,3-dihydrobenzofurans.

A. Nishida, M. Arisawa, Yukiyoshi Terada, 2004, Angewandte Chemie.

One-pot enyne metathesis/Diels-Alder/oxidation to six-membered silacycles with a multi-ring core: discovery of novel fluorophores.

Y. Fujii, T. Uno, M. Arisawa, 2017, Chemical communications.

Design and synthesis of indomethacin analogues that inhibit P-glycoprotein and/or multidrug resistant protein without COX inhibitory activity.

S. Shuto, Yoshihiro Ito, Koujirou Yamamoto, 2012, Journal of medicinal chemistry.

Conformationally Restricted GABA with Bicyclo[3.1.0]hexane Backbone as the First Highly Selective BGT-1 Inhibitor.

S. Shuto, H. Fukuda, H. Abe, 2014, ACS medicinal chemistry letters.

Cyclopropane-Based Peptidomimetics Mimicking Wide-Ranging Secondary Structures of Peptides: Conformational Analysis and Their Use in Rational Ligand Optimization.

S. Shuto, S. Yamada, T. Kameda, 2017, Chemistry.

Three-dimensional structural diversity-oriented peptidomimetics based on the cyclopropylic strain.

S. Shuto, S. Yamada, Y. Kogami, 2013, Organic letters.

Synthesis of Chiral cis-Cyclopropane Bearing Indole and Chromone as Potential TNFα Inhibitors.

S. Shuto, T. Matsuda, H. Fukuda, 2018, The Journal of organic chemistry.

Design and synthesis of histamine H3/H4 receptor ligands with a cyclopropane scaffold.

S. Shuto, S. Yamada, H. Fukuda, 2018, Bioorganic & medicinal chemistry letters.

Conformational restriction approach to β-secretase (BACE1) inhibitors III: effective investigation of the binding mode by combinational use of X-ray analysis, isothermal titration calorimetry and theoretical calculations.

Kenichiro Fujiwara, Kazunari Hattori, Hiroshi Takemoto, 2013, Bioorganic & medicinal chemistry.

Potent proteasome inhibitors derived from the unnatural cis-cyclopropane isomer of Belactosin A: synthesis, biological activity, and mode of action.

S. Shuto, M. Groll, A. Asai, 2013, Journal of medicinal chemistry.

Conformational restriction approach to β-secretase (BACE1) inhibitors: effect of a cyclopropane ring to induce an alternative binding mode.

S. Shuto, T. Yutsudo, Yoshikazu Tanaka, 2012, Journal of medicinal chemistry.

Alkene isomerization/enamide-ene and diene metathesis for the construction of indoles, quinolines, benzofurans and chromenes with a chiral cyclopropane substituent.

S. Shuto, M. Arisawa, Takaaki Kobayashi, 2011, Organic & biomolecular chemistry.

Carbon–Carbon Bond Formation between N-Heterocyclic Carbene Ligand on Ruthenium Carbene Catalysts and 1,4-Naphthoquinone via Intramolecular Carbon(sp3)–Hydrogen Bond Activation

T. Hibi, M. Arisawa, S. Aoki, 2021, Organometallics.

Design, Synthesis, and Monoamine Oxidase B Selective Inhibitory Activity of N-Arylated Heliamine Analogues.

K. Harada, K. Nunomura, M. Arai, 2022, ACS medicinal chemistry letters.

Oxidative Rearrangement of Primary Amines Using PhI(OAc)2 and Cs2CO3.

M. Arisawa, Kenichi Murai, Wataru Yamakoshi, 2019, Organic letters.

A New Tetracyclic Bromopyrrole-Imidazole Derivative through Direct Chemical Diversification of Substances Present in Natural Product Extract from Marine Sponge Petrosia (Strongylophora) sp.

K. Harada, M. Arai, M. Arisawa, 2022, Molecules.

Construction of a chiral quaternary carbon center by a radical cyclization/ring-enlargement reaction: synthesis of 4α-azidoethyl carbocyclic ribose, a key unit for the synthesis of cyclic ADP-ribose derivatives of biological importance

S. Shuto, H. Fukuda, Takatoshi Sato, 2015 .

Stereoselectivity in ring-closing olefin metathesis (RCM) of tethered dihexenoyl derivatives

A. Nishida, M. Arisawa, M. Nakagawa, 2002 .

Highly Sensitive Measurement of Inositol 1,4,5‐Trisphosphate by Using a New Fluorescent Ligand and Ligand Binding Domain Combination

S. Shuto, M. Arisawa, A. Tanimura, 2016, Chembiochem : a European journal of chemical biology.

Design and synthesis of indole derivatives of adenophostin A. A entry into subtype-selective IP3 receptor ligands

S. Shuto, Yoshihiro Ito, Mika Ito, 2010 .

Revisiting Chiral Recognition Mechanism on Chicken Alpha 1-Acid Glycoprotein: Location of Chiral Binding Sites and Insight into Chiral Binding Mechanism

J. Haginaka, M. Arisawa, Taku Yamashita, 2021, Separations.

Palladium‐Nanoparticle‐Catalyzed 1,7‐Palladium Migration Involving C—H Activation, Followed by Intramolecular Amination: Regioselective Synthesis of N1‐Arylbenzotriazoles and an Evaluation of Their Inhibitory Activity Toward Indoleamine 2,3‐Dioxygenase.

S. Shuto, H. Sugimoto, J. Wouters, 2014 .

SF3B2-mediated RNA splicing drives human prostate cancer progression.

Y. Kaneda, Jun Luo, N. Nonomura, 2019, Cancer research.

Recent developments in marine indole alkaloid synthesis.

A. Nishida, M. Arisawa, Toshiaki Nagata, 2003, Advances in experimental medicine and biology.

Design and Synthesis of Ether Derivatives of Spliceostatin A and their Biological Evaluation towards Prostate Cancer Treatment

K. Nunomura, N. Ohta, Keisuke Nimura, 2022, Tetrahedron Letters.

[Development of intramolecular oxidative phenolic coupling reactions using hypervalent iodine (III) reagents and their application to the synthesis of Amaryllidaceae alkaloids].

Y. Kita, M. Arisawa, H. Tohma, 2000, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.

Total Synthesis of Ansellone G and Phorbadione.

N. Kishimoto, Kanae Nakahara, M. Arisawa, 2022, The Journal of organic chemistry.

Structure-activity Relationship of Indomethacin Derivatives as IDO1 Inhibitors

S. Shuto, M. Arisawa, Motohiro Tanaka, 2021, AntiCancer Research.

Recent Advances in Metal-Nanoparticle-Catalyzed Coupling Reactions Assisted by Microwave Irradiation

M. Arisawa, M. Sako, 2021, Synthesis.

Ligand-free Suzuki–Miyaura coupling reaction of an aryl chloride using a continuous irradiation type microwave and a palladium nanoparticle catalyst: effect of a co-existing solid

T. Honma, M. Arisawa, Kenichi Murai, 2019, Green Chemistry.

Recent topics on reusable immobilized iron nanoparticle pre-catalysts

M. Arisawa, Makito Yamada, 2020 .

Tricarboxylic acid cycle activity suppresses acetylation of mitochondrial proteins during early embryonic development in Caenorhabditis elegans

A. Fukamizu, M. Matsumoto, H. Daitoku, 2019, The Journal of Biological Chemistry.

A method for cleaving an allyl protecting group at the amide nitrogen of peptides by one-pot olefin isomerization-oxidation.

S. Shuto, M. Arisawa, Kouki Kajihara, 2008, The Journal of organic chemistry.

Design and synthesis of 4-acetoxypentanamide derivatives of spliceostatin A and their biological evaluation towards prostate cancer treatment.

K. Nunomura, Keisuke Nimura, M. Arisawa, 2023, Bioorganic & medicinal chemistry letters.

Oxidative Intramolecular Phenolic Coupling Reaction Induced by a Hypervalent Iodine(III) Reagent: Leading to Galanthamine-Type Amaryllidaceae Alkaloids.

Y. Kita, M. Arisawa, M. Nakajima, 1999 .

Rational hopping of a peptidic scaffold into non-peptidic scaffolds: structurally novel potent proteasome inhibitors derived from a natural product, belactosin A.

T. Hirokawa, S. Shuto, A. Asai, 2014, Chemical communications.

Lewis Acid-Promoted Coupling Reactions of Acid Chlorides with Organoaluminum and Organozinc Reagents.

A. Nishida, M. Arisawa, M. Nakagawa, 1997, The Journal of organic chemistry.

Palladium-Catalyzed Seven-Membered Silacycle Construction: 1,7-Enyne Hydroxycyclization To Give a Benzosilepine Skeleton.

M. Arisawa, H. Fujioka, Shohei Yoshioka, 2018, Organic letters.

Substrate-Assisted Reductive Elimination Determining the Catalytic Cycle: A Theoretical Study on the Ni-Catalyzed 2,3-Disubstituted Benzofuran Synthesis via C–O Bond Activation

J. Hasegawa, M. Arisawa, Takeyuki Suzuki, 2022, Organometallics.

Double Ring Expansion Strategy for Fused 3-Benzazepines: Alternative Synthesis of the Dolby-Weinreb Enamine.

H. Aoyama, M. Arisawa, Kenichi Murai, 2022, The Journal of organic chemistry.

Direct synthesis of dialkylarylvinylsilane derivatives: metathesis of dialkylaryl-iso-propenylsilane and its application to tetracyclic silacycle dye synthesis.

Y. Tsutsumi, T. Uno, M. Arisawa, 2019, Chemical communications.

Cyclizations of benzo-fused substrates involving two multiple bonds, including heteroatom-substituted unsaturated bonds.

M. Arisawa, Shohei Ohno, 2020, The Journal of organic chemistry.

Development of Cycloisomerization with Rearrangement of a Tosyl Group Using N-Tosyl-o-allenylaniline.

M. Arisawa, Takeyuki Suzuki, Shohei Yoshioka, 2023, Journal of Organic Chemistry.

Palladium-Catalyzed Intramolecular Migratory Cycloisomerization of 3-Phenoxy Acrylic Acid Ester via C-O Bond Cleavage and C-O/C-C Bonds Formation for 2,3-Disubstituted Benzofurans Synthesis.

M. Arisawa, Kenichi Murai, M. Sako, 2023, Chemical & pharmaceutical bulletin.

Hard x-ray photoemission spectroscopic investigation of palladium catalysts immobilized on a GaAs(001) surface

S. Shuto, H. Yoshikawa, M. Shimoda, 2010 .

Structure determination of Pd-catalyst supported on S-terminated GaAs(001) using DFT calculation

S. Shuto, S. Tsukamoto, A. Ishii, 2010 .

Novel Organopalladium Material Formed on a Sulfur-Terminated GaAs(001) Surface

M. Pristovsek, M. Shimoda, S. Tsukamoto, 2002 .

Highly Reactive Organopalladium Catalyst Formed on Sulfur-Terminated GaAs(001)-(2 ×6) Surface

Y. Arakawa, M. Shimoda, S. Tsukamoto, 2006 .

Design and synthesis of N1,N8-diacetylspermidine analogues having a linker with desired functional groups.

M. Arisawa, A. Oguro, H. Fujioka, 2019, Organic & biomolecular chemistry.

Synthesis and Biological Evaluation of Simplified Ansellone Analogues with Lipophilic Side Chains as HIV-Latency-Reversing Agents.

N. Kishimoto, Kanae Nakahara, M. Arisawa, 2023, Chemistry.

Discovery of novel aldose reductase inhibitors using a protein structure-based approach: 3D-database search followed by design and synthesis.

M. Mizutani, N. Tomioka, A. Itai, 2001, Journal of medicinal chemistry.

Design, Synthesis, and Identification of 4″α-Azidoethyl-cyclic ADP-Carbocyclic-ribose as a Highly Potent Analogue of Cyclic ADP-Ribose, a Ca(2+)-Mobilizing Second Messenger.

S. Shuto, T. Kameda, H. Fukuda, 2016, Journal of medicinal chemistry.

Ligand-free Suzuki–Miyaura coupling using ruthenium(0) nanoparticles and a continuously irradiating microwave system

Y. Tamenori, M. Arisawa, Nozomi Saito, 2017 .

Iridium-Catalyzed Intramolecular Cycloisomerization between Functionalized Alkyne with Aryl Vinyl Ether: Synthesis of 2-Vinyl-3-Functionalized Methyl-Benzofurans.

M. Arisawa, Kenichi Murai, Takeyuki Suzuki, 2020, Journal of Organic Chemistry.

Design and synthesis of the stabilized analogs of belactosin A with the unnatural cis-cyclopropane structure.

S. Shuto, A. Asai, Y. Unno, 2013, Organic & biomolecular chemistry.

Three-dimensional structural diversity-oriented peptidomimetics based on the cyclopropylic strain.

S. Shuto, S. Yamada, Y. Kogami, 2013, Organic letters.

Opus: University of Bath Online Publication Store Design, Synthesis, and Chemical and Biological Properties of Cyclic Adp-4-thioribose as a Stable Equivalent of Cyclic Adp-ribose

T. Hirokawa, S. Shuto, B. Potter, 2022 .

Impact of helical elongation of symmetric oxa[n]helicenes on their structural, photophysical, and chiroptical characteristics.

M. Arisawa, M. S. Salem, Shinobu Takizawa, 2024, Chirality.