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・S. Zhang, M. Bao, M. Arisawa, M. Yamaguchi
Linking Chemical Reactions and
silica Nanoparticle Contact Using Synthetic Molecules
Chin. J. Chem., 42, 1781-1796, (2024).
DOI: 10.1002/cjoc.202300748
・K. Fukumoto, M. Yazaki, M. Arisawa
Synthesis of Unprotected Cyclic Peptide Methylene Dithioacetals by Rhodium-Catalyzed Oxidation of Methanol to Formaldehyde
Org. Lett.26, 221-224, (2024).
DOI: 10.1021/acsorglett3c03872
・W. Afrin, N. Yamada, S. Furuya, K. Yamamoto
Characterization of glutathione-specific gamma glutamyl cyclotransferase (ChaC) in Bombyx mori
Arch. Insect Biochem. Physiol. 114, e22027, (2023).
DOI: 10.1002/arch.22027
・M. Arisawa
Design, Synthesis, and Biological Activity of Small Organic Molecules for Environmental Stress Response
J. Synth. Org. Chem. Japan 81, 733, (2023).
DOI: 10.5059/yukigoseikyokaishi.81.733
・L. Antypenko, O. Antypenko, I. Kamaukh, O. Rebets, S. Kovalenko, M. Arisawa
5,6-Dihydrotetrazolo[1,5-c]quinazolines: Toxicity Prediction, Synthesis, Antimicrobial Activity, Molecular Docking and Perspectives
Arch. Pharm, 356, e2300029, (2023).
DOI: 10.1002/ardp.202300029
・塚越駿，岩田和樹，花田博幸，笹野遼平，竹内一郎，魚住信之，有澤美枝子
論文テキストを用いた化合物探索の漸進的効率化
研究報告自然言語処理(NL), 256(13), (2023).
・T. Kaneko, Y. Mita, K. Nozawa-Kumada, M. Yazaki, M. Arisawa, E. Niki, N. Noguchi, Y. Saito
Antioxidant Action of Persulfides and Polysulfides Against Free Radical-Mediated Lipid Peroxidation
J. Radic., Res., 56, 677, (2023).
DOI: 10.1080/10715762.2023.2165918
・L. Antypenko, F. Meyer, Z. Sadyk, K. Shabelnyk, S.Kovalenko, K. G. Steffens, L.-A. Garbe
Combined Application of Tacrolimus with Cyproconazole, Hymexazol and Novel {2-(3-R-1H-1,2,4-triazol-5-yl)phenyl}amines as Antifungals: In vitro Growth Inhibition and In Silico Molecular Docking Analysis to Fungal Chitin Deacetylase
J. Fungi, 9, 79, (2023).
DOI: 10.3390/jof9010079
・Y. Wang, R. Segawa, Y. Weng, K. Nakai, K. Ohashi, M. Hiratsuka, M. Arisawa, N. Hirasawa
Selective Induction of Thymic Stromal Lymphopoietin Expression by Novel Nitrogen-Containing Steroid Compounds in PAM-212 Cells
J. Transl. Autoimmun., 6, 100186, (2023).
DOI: 10.1016/j.jtauto.2022.100186
・S. Zhang, M. Bao, M. Arisawa, M. Yamaguchi
Stable and Unstable Concentration Oscillations Induced by Temperature Oscillations on Reversible Noneequilibrium Chemical Reactions of Helicene Oligomers
Int. J. Mol. Sci., 24, 693, (2023).
DOI: 10.3390/ijms24010693
・K. Fukumoto, M. Yazaki, M. Arisawa
Rhodium-Catalyzed Synthesis of Peptide Polysulfides by Insertion of Sulfur into Unprotected Peptide Disulfides
Org. Lett., 24, 8176-8179, (2022).
DOI: 10.1021/acs.orglett.2c03257
・K. Fukumoto, M. Yazaki, M. Arisawa
Rhodium-Catalyzed Insertion Reaction of Perfluoroarenes into Unprotected Peptide Disulfides
Asian J. Org. Chem., 11, e202200340, (2022).
DOI: 10.1021/acs.orglett.1c03485
・K. Yamamoto, N. Yamada, S. Endo, K. Kurogi, Y. Sakakibara, M. Suiko
Novel Silkworm (Bombyx mori) Sulfotransferase swSULT ST3 Is Involved in Metabolism of Polyphenols From Mulberry Leaves
PLoS One, 17, e0270804, (2022).
DOI: 10.1021/acs.orglett.1c03485
・M. Arisawa
Development of Biostimulants and Pharmaceuticals Using Synthetic Heavy-Heteroatom Organic Compounds
J. of SJWS, 22, 69-79, (2022).
DOI:10.5939/sjws.220014
・M. Arisawa,T. Mizuno, K. Nozawa-Kumada, K. Itto-Nakama, M. Furuta, and S. Tanii
Rhodium-Catalyzed Synthesis of Unsymmetric Di(heteroaryl)ureas Involving Equilibrium Shift
Org. Lett, 23, 9382-9386, (2021).
DOI: 10.1021/acs.orglett.1c03485
・M. Arisawa and M. Yamaguchi
Thiiranes and Thiirenes-Fused Ring Derivatives
Comprehensive Heterocyclic Chemistry IV, 1, 413-435, (2021).
ISBN978-0-12-818656-5
・M. Arisawa M. Yoshida, K. Fukumoto, T. Sawato, M. Yamaguchi, M. Matsubara, and K. Kanie
Three-state Structural Switching and Selective Molecular Interactions of Cylindrical Concentric Monodomain Liquid Crystal Elastomer
Chemistry Select., 6, 12604-12609, (2021).
DOI: 10.1002/slct202103490
・M. Arisawa, R. Iwamoto, and M. Yamaguchi
Unstable ansd Stable Thermal Hysteresis Under Thermal Triangle Waves
Chemistry Select., 30, 4461-4465, (2021).
DOI: 10.1002/slct202100089
・M. Arisawa and M. Yamaguchi
有機合成のための新触媒反応101
有機合成化学協会, (2021) (執筆担当)
ISBN978-4-8079-2005-1
・M. Arisawa, K. Fukumoto, M. Yamaguchi
Rhodium-Catalyzed Oxidation of Unprotected Peptide Thiols to Disulfides with Oxygen in Water
ACS, Catal., 10, 15060-15064, (2020).
DOI: 10.1021/acscatal.0c04799
・M. Arisawa
Transition-Metal-Catalyzed Synthesis of Organohosphorus Compounds Involving P-P Bond Cleavage
Synthesis, 52, 2795-2806, (2020).
DOI: 10.1055/s-0040-1707890
・M. Arisawa and M. Yamaguchi
Rhodium-catalyzed Synthesis of Organosulfur Compound Involving S-S Bond Cleavage of Disulfides and Sulfer
Molecules, 25, 3595-3630, (2020).
DOI: 10.3390/molecules25163595
・M. Arisawa, K. Fukumoto and M. Yamaguchi
Rhodium-catalyzed phosphorylation reaction of water-soluble disulfides using hypodiphosphoric acid tetraalkyl esters in water
RSC Adv., 10, 13820-13823 (2020).
DOI: 10.1039/D0RA02377A
・M. Arisawa, R. Suzuki, K. Ohashi and M. Yamaguchi
Rhodium‐Catalyzed Synthesis of Heteroarylselenyl Esters from Diheteroaryl Diselenides and Acid Fluorides
Asian J. Org. Chem., 9, 553-556 (2020).
DOI: 10.1002/ajoc.202000077
・M. Arisawa, K. Nakai, T. Yamada, R. Suzuki and M. Yamaguchi
Synthesis of Cycloalkyl/steroidal Heteroaryl Sulfides Using Rhodium-Catalyzed Heteroaryl Exchange Reaction
Heterocycles, 100, 104-118 (2020).
DOI: 10.3987/COM-19-14147
・T. Sawato, M. Arisawa and M. Yamaguchi
Reversible Formation of Self-assembly Gels Containing Giant Vesicles in Vesicles in Trifluoromethylbenzene Using Oxymethylenehelicene Oligomers with Terminal C16 Alkyl Groups
Bull. Chem. Soc. Jpn., 93, 1497-1503 (2020).
DOI: 10.1246/bcsj.20200164
・M. Arisawa and M. Yamaguchi
Rhodium-Catalyzed Synthesis of Organosulfur Compounds using Sulfur
Synlett, 30, 1621-1631 (2019).
DOI: 10.1055/s-0037-1611867
・M. Arisawa
Rhodium-catalyzed synthesis of unsymmetric di(heteroaryl) compounds via heteroaryl exchange reactions
Phsphorus, Sulfur, and Silicon and the Related Elements, 194, 643-648 (2019).
DOI: 10.1080/10426507.2019.1602621
・W. Ichinnose, T. Sawato, H. Kitano, Y. Shinozaki, M. Arisawa, N. Saito, T. Yoshikawa and M. Yamaguchi
Optically active iodohelicene derivatives exhibit histamine N-methyl transferase inhibitory activity
J. Antibiot., 72, 476-481 (2019).
DOI: 10.1038/s41429-018-0118-z
・S. Tanii, M. Arisawa and M. Yamaguchi
Acid-catalyzed synthesis of condensed polycyclic diaryl ethers from arenols
Chem. Commun., 55, 14078-14080 (2019).
DOI: 10.1039/c9cc07172e
・M. Arisawa, T. Tazawa, W. Ichinose, H. Kobayashi and M. Yamaguchi
Rhodium‐Catalyzed Synthesis of Dialkyl (Heteroaryl) Phosphine Sulfides by Phosphinylation of Heteroaryl Sulfides
Adv. Synth. Catal., 360, 3488-3491 (2018).
DOI: 10.1002/adsc.201800630
・M. Arisawa, K. Sawahata, T. Ichikawa and M. Yamaguchi
Rhodium-Catalyzed Isomerization and Alkyne Exchange Reactions of 1,4-Dithiins via the 1,2-Ethenedithiolato Rhodium Complex
Organometallics, 37, 3174-3180 (2018).
DOI: 10.1021/acs.organomet.8b00498
・S. Tanii, M. Arisawa, T. Tougo and M. Yamaguchi
Catalytic Method for the Synthesis of C-N-Linked Bi(heteroaryl)s Using Heteroaryl Ethers and N-Benzoyl Heteroarene
Org. Lett., 20, 1756-1759 (2018).
DOI: 10.1021/acs.orglett.8b00245
・M. Arisawa, K. Sawahata, T. Yamada, D. Sarkar and M. Yamaguchi
Rhodium-Catalyzed Insertion Reaction of PhP Group of Pentaphenylcyclopentaphosphine with Acyclic and Cyclic Disulfides
Org. Lett., 20, 938-941 (2018).
DOI: 10.1021/acs.orglett.7b03825
・M. Arisawa, S. Tanii, T. Tazawa, and M. Yamaguchi
Synthesis of Unsymmetric HetAr?X?HetAr’ Compounds by Rhodium-Catalyzed Heteroaryl Exchange Reactions
Heterocycles, 94, 2179-2207 (2017).
DOI: 10.3987/REV-17-869
・M. Arisawa, T. Tazawa, S. Tanii, K. Horiuchi, and M. Yamaguchi
Rhodium-Catalyzed Synthesis of Unsymmetric Di(heteroaryl) Sulfides Using Heteroaryl Ethers and S-Heteroaryl Thioesters via Heteroarylthio Exchange
J. Org. Chem., 82, 804-810 (2017).
DOI: 10.1021/acs.joc.6b02585
・S. Tanii, M. Arisawa, T. Tougo, K. Horiuchi, and M. Yamaguchi
Thieme Chemistry Journals Awardees ? Where Are They Now? Rhodium-Catalyzed Synthesis of Unsymmetric Di (heteroaryl) Ethers Using Heteroaryl Exchange Reaction
Synlett, 28, 1601-1607 (2017).
DOI: 10.1055/s-0036-1588801
・T. Sawato, A. Yagi, M. Ariaswa, and M. Yamaguchi
Chemical braking exhibited by ethynylhelicene (M)-nonamer in solution: Competitive reaction system of self-catalysis to form double-helix and approach towards equilibrium to form random-coil
Tetrahedron, 73, 2801-2805 (2017).
DOI: 10.1016/j.tet.2017.03.083
・M. Yamaguchi, M. Arisawa, M. Shigeno, and N. Saito
Equilibrum and Nonequilibrium Chemical Reactions of Helicene Oligomers in the Noncovalent Bond Formation
Bull Chem. Soc. Jpn., 89, 1145-1169 (2016).
DOI: 10.1246/bcsj.20160133
・M. Arisawa, T. Yamada, S. Tanii, Y. Kawada, H. Hashimoto and M. Yamaguchi
Rhodium-catalyzed P?P bond exchange reaction of diphosphine disulfides
Chem. Commun., 52, 13580-13583 (2016).
DOI: 10.1039/c6cc07302f
・M. Arisawa, S. Tanii, T. Tazawa, and M. Yamaguchi
Rhodium-Catalyzed Transformation of Heteroaryl Aryl Ethers to Heteroaryl Fluorides
Chem. Commun., 52, 11390-11393 (2016).
DOI: 10.1039/c6cc05400e
・M. Arisawa, T. Ichikawa, S. Tanii and M. Yamaguchi
Synthesis of Symmetrical and Unsymmetrical 1,4-Dithiins by Rhodium-Catalyzed Sulfur Addition Reaction to Alkynes
Synthesis, 48, 3107-3119 (2016).
DOI: 10.1055/s-0035-1561452
・M. Arisawa, T. Ichikawa, and M. Yamaguchi
Synthesis of Thiiranes by Rhodium-Catalyzed Sulfur Addition Reaction to Reactive Alkenes
Chem. Commun., 51, 8821-8824 (2015).
DOI: 10.1039/C5CC01570G
・M. Arisawa, Y. Nihei, and M. Yamaguchi
Rhodium-Catalyzed 2-Methylthiolation Reaction of Thiazoles/Oxazoles Using 2-(Methylthio)Thizole
Heterocycles, 90, 939-949 (2015).
DOI: 10.3987/COM-14-S(K)59
・M. Arisawa, S. Tanii, T. Yamada and M. Yamaguchi
Palladium-catalyzed Addition Reaction of Thioesters to Norbornenes
Tetrahedron, 71, 6449-6458 (2015).
DOI: 10.1016/j.tet.2015.05.042
・M. Miyagawa, M. Arisawa and M. Yamaguchi
Equilibrium Shift Induced by Chiral Nanoparticle Precipitation in Rhodium-Catalized Disulfide Exchange Reaction
Tetrahedron, 71, 4920-4926 (2015).
DOI: 10.1016/j.tet.2015.05.106
・M. Arisawa, S. Tanii, and M. Yamaguchi
A Palladium-Catalyzed Addition Reaction of Aroyl/Heteroaroyl Acid Anhydrides to Norbornenes
Chem. Commun., 50, 15267-15270 (2014).
DOI: 10.1039/C4CC07759H
・G. Li, M. Arisawa and M. Yamaguchi
Rhodium-catalyzed Synthesis of Unsymmetrical Di (Aryl/Heteroaryl) Methanes Using Aryl/Heteroarylmethyl Ketons via CO-C Bond Cleavage
Chem. Commun., 50, 4328-4330 (2014).
DOI: 10.1039/C4CC00816B
・M. Arisawa
Synthesisof organosulfides using Synthesis of organosulfides using transition-metal-catalyzed substitution reactions: to construct exergonic reactions employing metal inorganic and organic co-substrate/co-product methods
Tetrahedron Lett., 55, 3391-3399 (2014).
DOI: 10.1016/j.tetlet.2014.04.081
・G. Li, M. Arisawa, and M. Yamaguchi
Rhodium-Catalyzed Synthesis and Reactions of N-Acylphthalimides
Asian J. Org. Chem., 2, 983-988 (2013).
DOI: 10.1002/ajoc.201300094
・M. Arisawa, G. Li, and M. Yamaguchi
Rhodium-Catalyzed Synthesis of 2,3-Diaryl-1,4-Diketones via Oxidative Coupling of Benzyl Ketones Using α-Thioketone Oxidizing Reagent
Tetrahedron Lett., 54, 1298-1301 (2013).
DOI: 10.1016/j.tetlet.2012.12.107
・M. Arisawa, T. Ichikawa, and M. Yamaguchi
Synthesis of Unsymmetrical Polyfluorinated Diaryl Dulfides by Rhodium-Catalyzed aryl Exchange Reaction
Tetrahedron Lett., 54, 4327-4329 (2013).
DOI: 10.1016/j.tetlet.2013.06.021
・M. Arisawa, S. Nakane, M. Kuwajima, and M. Yamaguchi
Rhodium-Catalyzed Synthesis of Benzofurans by the Reaction of Ketones and O-Difluoeobenzenes
Heterocycles, 86, 1103-1118 (2012).
DOI: 10.3987/COM-12-S(N)57
・M. Arisawa, T. Ichikawa, and M. Yamaguchi
Rhodium-Catalyzed Synthesis of Diaryl Sulfides Using Aryl Fluorides and Sulfur/Organopolysulfides
Org. Lett., 14, 5318-5321 (2012).
DOI: 10.1021/ol302497m
・M. Arisawa, Y. Nihei and M. Yamaguchi
Rhodium-Catalyzed Arylthiolation Reaction of Nitroalkanes, Diethyl Malonate, and 1,2- Diphenylethanone with Diaryl Disulfides: Control of Disfavored Equilibrium Reaction
Tetrahedron Lett., 53, 5729-5732 (2012).
DOI: 10.1016/j.tetlet.2012.07.132
・M. Arisawa, M. Kuwajima, F. Toriyama, G. Li and M. Yamaguchi
Rhodium-Catalyzed Acyl-Transfer Reaction between Benzyl Ketones and Thioesters: Synthesis of Unsymmetric Ketones by Ketone CO-C Bond Cleavage and Intermolecular Rearrangement
Org. Lett., 14, 3804-3807 (2012).
DOI: 10.1021/ol3017148
・M. Arisawa, Y. Nihei, T. Suzuki, and M. Yamaguchi
Rhodium-Catalyzed Cleavage Reaction of Aryl Methyl Ethers with Thioesters
Org. Lett., 14, 855-857 (2012).
DOI: 10.1021/ol2033724
・M. Arisawa, Y. Igarashi, H. Kobayashi, T.Yamada, K. Bando, T. Ichikawa and M. Yamaguchi
Equilibrium Shift in the Rhodium-catalyzed Acyl Transfer Reactions
Tetrahedron, 67, 7846-7859 (2011).
DOI: 10.1016/j.tet.2011.07.031
・H. Cho, Y. Yasui, S. Kobayashi, E. Kwon, M. Arisawa and M. Yamaguchi
Synthesis and Substitution Reactions of 4(6)-Chloro-dihydropyrimidines
Heterocycles, 83, 1807-1818 (2011).
DOI: 10.3987/COM-11-12244
・M. Arisawa, F. Toriyama and M. Yamaguchi
Rhodium-catalyzed Phenylthiolation Reaction of Heteroaromatic Compounds using α-(phenylthio) isobutyrophenone
Tetrahedron Lett., 52, 2344-2347 (2011).
DOI: 10.1016/j.tetlet.2011.02.077
・M. Arisawa, T. Watanabe and M. Yamaguchi
Direct Transformation of Organosulfur Compounds to Organophosphorus Compounds: Rhodium- catalyzed Synthesis of 1-Alkynylphosphine Sulfides and Acylphosphine Sulfides
Tetrahedron Lett., 52, 2410-2412 (2011).
DOI: 10.1016/j.tetlet.2011.02.112
・M. Arisawa, F. Toriyama and M. Yamaguchi
Rhodium-catalyzed α-Methylthiolation Reaction of Unactivated Ketones Using 1,2-Diphenyl-2- Methylthio-1-Ethanone for the Methylthio Transfer Reagent
Tetrahedron, 67, 2305-2312 (2011).
DOI :10.1016/j.tet.2011.01.071
・M. Arisawa, Y. Igarashi, Y. Tagami, M. Yamaguchi and C. Kabuto
Rhodium-catalyzed Carbothiolation Reaction of 1-Alkylthio-1-Alkynes
Tetrahedron Lett., 52, 920-922 (2011).
DOI: 10.1016/j.tetlet.2010.12.065
・M. Arisawa, F. Toriyama and M. Yamaguchi
An Activated Catalyst RhH(PPh3)4-dppe-Me2S2 for α-Methylthiolation of ?-Phenyl Ketones
Heteroatom Chem., 22, 18-23 (2011).
DOI: 10.1002/hc.20650
・M. Arisawa, M. Kuwajima and M. Yamaguchi
Synthesis of o-(diphenylphosphinoyloxy)anilines by the Rhodium-Catalyzed Reaction of Nitroarenes and Diphenylphosphine Oxide
Tetrahedron Lett., 51, 3116-3118 (2010).
DOI: 10.1016/j.tetlet.2010.04.029
・M. Arisawa, T. Yamada and M. Yamaguchi
Rhodium-Catalyzed Interconversion between Acid Fluorides and Thioesters Controlled using Heteroatom Acceptors
Tetrahedron Lett., 51, 6090-6092 (2010).
DOI: 10.1016/j.tetlet.2010.09.009
・M. Arisawa, F. Toriyama and M. Yamaguchi
Rhodium-Catalyzed Organothio Exchange Reaction of Alphaα-Organothioketones with Disulfides
Chem. Phar. Bull., 58, 1349-1352 (2010)
DOI: 10.1248/cpb.58.1349
・M. Arisawa, T. Yamada and M. Yamaguchi
Synthesis of Acylphosphine Sulfides by Rhodium-Catalyzed Reaction of Acid Fluorides and Diphosphine Disulfides
Tetrahedron Lett., 51, 4957-4958 (2010).
DOI: 10.1016/j.tetlet.2010.07.038
・M. Arisawa and M. Yamaguchi
Metal-Catalyzed Phosphinyl Ester Forming Reaction of Alcohols and Phenols with Diphosphine Disulfides and a Dioxide
Tetrahedron Lett., 51, 4840-4842 (2010).
DOI: 10.1016/j.tetlet.2010.07.040
・M. Arisawa, M. Kuwajima, A. Suwa and M. Yamaguchi
RhCl3-Catalyzed Disulfide Exchange Reaction of Insulfin and Dithiodiglycolic Acid
Heterocycles, 80, 1239-1248 (2010).
DOI: 10.3987/COM-09-S(S)110
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