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65. Transient π-Coordination Enables Nucleophilic Borylation of Simple Arenes
65. Transient π-Coordination Enables Nucleophilic Borylation of Simple Arenes
Mutoh, Y.; Khalaf, R.; Asako, S.; Ilies, L.
Chem. Sci. 2026, 17 (1), 664–670. DOI: 10.1039/D5SC08107F
An initial version of this work was deposited in ChemRxiv on April 22, 2025. DOI: 10.26434/chemrxiv-2025-bszc1-v3
Featured in the themed collection: Most popular 2025 organic synthesis articles
63. Activation of aryl chlorides through π-coordination for radical coupling with arenes
63. Activation of aryl chlorides through π-coordination for radical coupling with arenes
Nagata, M.; Itonaga, K.; Mutoh, Y.; Endo, K.; Ilies, L.
Chem. Lett. 2024, 53 (12), upae233. DOI: 10.1093/chemle/upae233
62. Conformational Control of [2]Rotaxane by Hydrogen Bond
62. Conformational Control of [2]Rotaxane by Hydrogen Bond
Kawasaki, Y.; Rashid, S.; Ikeyatsu, K.; Mutoh, Y.; Yoshigoe, Y.; Kikkawa, S.; Azumaya, I.; Hosoya, S.; Saito, S.
J. Org. Chem. 2022, 87 (9), 5744–5759 (Open Access). DOI: 10.1021/acs.joc.2c00086
61. The Aza-Prins Reaction of 1,2-Dicarbonyl Compounds with 3-Vinyltetrahydroquinolines: Application to the Synthesis of Polycyclic Spirooxindole Derivatives
61. The Aza-Prins Reaction of 1,2-Dicarbonyl Compounds with 3-Vinyltetrahydroquinolines: Application to the Synthesis of Polycyclic Spirooxindole Derivatives
Saito, S.; Katamura, T; Tsukazaki, R.; Fujisawa, A.; Yoshigoe, Y.; Mutoh, Y.
J. Org. Chem. 2021, 86 (23), 16425–16433 (Open Access). DOI: 10.1021/acs.joc.2c00086
60. Liquid-Crystalline 1,4-Benzoquinone Derivative: Self-Assembling Behavior and Redox Properties
60. Liquid-Crystalline 1,4-Benzoquinone Derivative: Self-Assembling Behavior and Redox Properties
Tamaki, S.; Mutoh, Y.; Isoda, K.
J. Mol. Liq. 2021, 338, 116636. DOI: 10.1016/j.molliq.2021.116636
59. Stimulus-Responsive Supercooled π-Conjugated Liquid and Its Application in Rewritable Media
59. Stimulus-Responsive Supercooled π-Conjugated Liquid and Its Application in Rewritable Media
Sato, Y.; Mutoh, Y.; Morishita, S.; Tsurumachi, N.; Isoda, K.
J. Phys. Chem. Lett. 2021, 12 (11), 3014–3018. DOI: 10.1021/jpclett.1c00247
Highlighted as a Supplementary Cover
58. Asymmetric N-heteroacene liquid showing site-selective acid sensing
58. Asymmetric N-heteroacene liquid showing site-selective acid sensing
Akiyama, Y.; Mutoh, Y.; Isoda, K.
J. Photochem. Photobiol., A 2020, 407, 113036. DOI: 10.1016/j.jphotochem.2020.113036
57. Synthesis and Systematic Structural Analysis of Cationic Half-Sandwich Ruthenium Chalcogenocarbonyl Complexes
57. Synthesis and Systematic Structural Analysis of Cationic Half-Sandwich Ruthenium Chalcogenocarbonyl Complexes
Suzuki, A.; Mutoh, Y.; Tsuchida, N.; Fung, C.-W.; Kikkawa, S.; Azumaya, I.; Saito, S.
Chem. - Eur. J. 2020, 26 (17), 3795–3802. DOI: 10.1002/chem.201904600
Featured in a Hot Topic: Carbon, Graphite, and Graphene.
56. Synthesis and properties of anionic ruthenium thionitrosyl and selenonitrosyl complexes that contain tetraanionic 2-hydroxybenzamidobenzene ligands
56. Synthesis and properties of anionic ruthenium thionitrosyl and selenonitrosyl complexes that contain tetraanionic 2-hydroxybenzamidobenzene ligands
Fung, C.-W.; Fukada, G.; Mutoh, Y.; Tsuchida, N.; Saito, S.
Dalton Trans. 2020, 49 (3), 613–624 (Open Access). DOI: 10.1039/c9dt04219a
Selected as a HOT Article
Highlighted in the Outside Front Cover (Dalton Trans. 2020, 49, 527. DOI: 10.1039/D0DT90012E)
55. Synthesis of Helical 3,3′-Bridged-2,2′-Bibenzo[g]quinolines
55. Synthesis of Helical 3,3′-Bridged-2,2′-Bibenzo[g]quinolines
Yamazaki, Y.; Mizuma, R.; Abe, H.; Aoki, R.; Mutoh, Y.; Saito, S.
Chem. Lett. 2020, 49 (2), 133–136. DOI: 10.1246/cl.190803
54. Synthesis of lactone-fused pyrroles by ruthenium-catalyzed 1,2-carbon migration-cycloisomerization
54. Synthesis of lactone-fused pyrroles by ruthenium-catalyzed 1,2-carbon migration-cycloisomerization
Watanabe, T.; Mutoh, Y.; Saito, S.
Org. Biomol. Chem. 2020, 18 (1), 81–85 (Open Access). DOI: 10.1039/C9OB02363A
Featured in the themed collection: Synthetic methodology in OBC
53. Suzuki−Miyaura Cross-Coupling of 1,8-Diaminonaphthalene (dan)-Protected Arylboronic Acids
53. Suzuki−Miyaura Cross-Coupling of 1,8-Diaminonaphthalene (dan)-Protected Arylboronic Acids
Mutoh, Y.; Yamamoto, K.; Saito, S.
ACS Catal. 2020, 10 (1), 352–357 (Letter). DOI: 10.1021/acscatal.9b03667
Highlighted as a Supplementary Cover
Ranked in the Top 9 Most Downloaded Article for the Previous 30 Days (20200116)
プレスリリース（日本語、リンク切れ）
52. Reversibly/Irreversibly Stimuli-Responsive Inks Based on N-Heteroacene Liquids
52. Reversibly/Irreversibly Stimuli-Responsive Inks Based on N-Heteroacene Liquids
Isoda, K.; Matsubara, M.; Ikenaga, A.; Akiyama, Y.; Mutoh, Y.
J. Mater. Chem. C 2019, 7 (45), 14075–14079 (Communication). DOI: 10.1039/C9TC05195C
51. Ruthenium-Catalyzed (Z)-Selective Hydroboration of Terminal Alkynes with Naphthalene-1,8-diaminatoborane
51. Ruthenium-Catalyzed (Z)-Selective Hydroboration of Terminal Alkynes with Naphthalene-1,8-diaminatoborane
Yamamoto, K.; Mohara, Y.; Mutoh, Y.; Saito, S.
J. Am. Chem. Soc. 2019, 141 (43), 17042–17047 (Communication, Open Access). DOI: 10.1021/jacs.9b06910
Highlighted as a Supplementary Cover
Highlighted in Synfacts (Synfacts 2019, 15 (12), 1405. DOI: 10.1055/s-0039-1691106)
50. One-dimensional single-helix coordination polymer self-assembled by a crown-ether appended-N-heteroacene radical anion
50. One-dimensional single-helix coordination polymer self-assembled by a crown-ether appended-N-heteroacene radical anion
Isoda, K.; Takahashi, H.; Mutoh, Y.; Hoshino, N.; Akutagawa, T.
Dalton Trans. 2019, 48 (35), 13125–13129 (Communication). DOI: 10.1039/C9DT02797A
Highlighted as an Inside Back Cover (Dalton Trans. 2019, 48 (35), 13493. DOI: 10.1039/C9DT90199J)
49. Stimuli-Responsive Room Temperature N-Heteroacene Liquid: In situ Observation of Self-Assembling Process and Its Multiple Properties
49. Stimuli-Responsive Room Temperature N-Heteroacene Liquid: In situ Observation of Self-Assembling Process and Its Multiple Properties
Isoda, K.; Ishiyama, T.; Mutoh, Y.; Matsukuma, D.
ACS Appl. Mater. Interfaces 2019, 11 (12), 12053–12062. DOI: 10.1021/acsami.8b21695
Highlighted as a Supplementary Cover
48. Evaluation of the Steric Bulk of Substituents Utilizing the Shuttling Behavior of [2]Rotaxanes with N-Arylpyrrole Moieties
48. Evaluation of the Steric Bulk of Substituents Utilizing the Shuttling Behavior of [2]Rotaxanes with N-Arylpyrrole Moieties
Yamashita, Y.; Saito, Y.; Kikkawa, S.; Mutoh, Y.; Hosoya, S.; Azumaya, I.; Saito, S.
Eur. J. Org. Chem. 2019, 2019 (21), 3412–3420. DOI: 10.1002/ejoc.201801476
Selected as a Very Important Paper (VIP)
Selected as a Cover Feature [Eur. J. Org. Chem. 2019, 2019, 3285 (Free Access). DOI: 10.1002/ejoc.201900595]
Invited contribution to the Special Issue "Dedicated to 50 Years of Rotaxanes"
47. Tuning Electronic Properties and Acid-Responsive Behavior of N-Heteroacene-based π-Conjugated Liquids by Changing the Number of π-Conjugated Substituents
47. Tuning Electronic Properties and Acid-Responsive Behavior of N-Heteroacene-based π-Conjugated Liquids by Changing the Number of π-Conjugated Substituents
Sato, Y.; Mutoh, Y.; Matsukuma, D.; Nakagawa, M; Kawai, T.; Isoda, K.
Chem. - Asian J. 2018, 13 (18), 2619–2625. DOI: 10.1002/asia.201800631
Selected as a Cover Feature [Chem. - Asian. J. 2018, 13 (18), 2574 (Free Access). DOI: 10.1002/asia.201800999]
46. Ruthenium-Catalyzed Cycloisomerization of 2-Alkynylstyrenes via 1,2-Carbon Migration that Leads to Substituted Naphthalenes
46. Ruthenium-Catalyzed Cycloisomerization of 2-Alkynylstyrenes via 1,2-Carbon Migration that Leads to Substituted Naphthalenes
Watanabe, T.; Abe, H.; Mutoh, Y.; Saito, S.
Chem. - Eur. J. 2018, 24 (45), 11545–11549 (Communication). DOI: 10.1002/chem.201802413
Selected as a Cover Feature [Chem. - Eur. J. 2018, 24 (45), 11515 (Free Access). DOI: 10.1002/chem.201803780]
45. (Z)-Selective Hydrosilylation of Terminal Alkynes with HSiMe(OSiMe3)2 Catalyzed by a Ruthenium Complex containing an N-Heterocyclic Carbene
45. (Z)-Selective Hydrosilylation of Terminal Alkynes with HSiMe(OSiMe3)2 Catalyzed by a Ruthenium Complex containing an N-Heterocyclic Carbene
Mutoh, Y.; Mohara, Y. Saito, S.
Org. Lett. 2017, 19 (19), 5204–5207 (Open Access). DOI: 10.1021/acs.orglett.7b02477
Highlighted in Organic Chemistry Portal
44. Synthesis of Mechanically Planar Chiral rac-[2]Rotaxanes by Partitioning of an Achiral [2]Rotaxane: Stereoinversion Induced by Shuttling
44. Synthesis of Mechanically Planar Chiral rac-[2]Rotaxanes by Partitioning of an Achiral [2]Rotaxane: Stereoinversion Induced by Shuttling
Mochizuki, Y.; Ikeyatsu, K.; Mutoh, Y.; Hosoya, S.; Saito, S.
Org. Lett. 2017, 19 (16), 4347–4350. DOI: 10.1021/acs.orglett.7b02043
43. Ruthenium-Catalyzed Cycloisomerization of 2-Alkynylanilides: Synthesis of 3-Substituted Indoles by 1,2-Carbon Migration
43. Ruthenium-Catalyzed Cycloisomerization of 2-Alkynylanilides: Synthesis of 3-Substituted Indoles by 1,2-Carbon Migration
Watanabe, T.; Mutoh, Y.; Saito, S.
J. Am. Chem. Soc. 2017, 139 (23), 7749–7752 (Communication, Open Access). DOI: 10.1021/jacs.7b04564
Ranked in the Top 12 Most downloaded Article for the previous 30 days (20170704)
42. Synthesis of [2]Catenanes by Intramolecular Sonogashira-Type Reaction
42. Synthesis of [2]Catenanes by Intramolecular Sonogashira-Type Reaction
Ito, K.; Mutoh, Y.; Saito, S.
J. Org. Chem. 2017, 82 (12), 6118–6124. DOI: 10.1021/acs.joc.7b00672
40. A Ruthenium Tellurocarbonyl (CTe) Complex with a Cyclopentadienyl Ligand: Systematic Studies of a Series of Chalcogenocarbonyl Complexes [CpRuCl(CE)(H2IMes)] (E = O, S, Se, Te)
40. A Ruthenium Tellurocarbonyl (CTe) Complex with a Cyclopentadienyl Ligand: Systematic Studies of a Series of Chalcogenocarbonyl Complexes [CpRuCl(CE)(H2IMes)] (E = O, S, Se, Te)
Suzuki, A.; Arai, T.; Ikenaga, K.; Mutoh, Y.; Tsuchida, N.; Saito, S.; Ishii, Y.
Dalton Trans. 2017, 46 (1), 44–48 (Communication). DOI: 10.1039/C6DT04440A
Featured in the themed web collection: Selenium & Tellurium chemistry at the beginning of the 3rd millennium: a celebration of ICCST
39. Synthesis and Shuttling Behavior of [2]Rotaxanes with a Pyrrole Moiety
39. Synthesis and Shuttling Behavior of [2]Rotaxanes with a Pyrrole Moiety
Matsuoka, Y.; Mutoh, Y.; Azumaya, I.; Kikkawa, S.; Kasama, T.; Saito, S.
J. Org. Chem. 2016, 81 (9), 3479–3487 (Featured Article, Editor's Choice, Open Access). DOI: 10.1021/acs.joc.5b02911
Highlighted in the Front Cover
Ranked in the Top 2 Most downloaded Article for the previous 30 days
Ranked in the Top 20 Most downloaded Article for the previous 12 months
38. Sequence-Selective Synthesis of Rotacatenane Isomers
38. Sequence-Selective Synthesis of Rotacatenane Isomers
Hayashi, R.; Slavík, P.; Mutoh, Y.; Kasama, T.; Saito, S.
J. Org. Chem. 2016, 81 (3), 1175–1184. DOI: 10.1021/acs.joc.5b02697
37. Synthesis of a Homochiral [2]Rotaxane from a BINOL-derived Macrocyclic Phenanthroline
37. Synthesis of a Homochiral [2]Rotaxane from a BINOL-derived Macrocyclic Phenanthroline
Saito, S.; Hirano, Y.; Mutoh, Y.; Kasama, T.
Chem. Lett. 2015, 44 (11), 1509–1511. DOI: 10.1246/cl.150693
36. Theoretical Study on Internal Alkyne/Vinylidene Isomerization in Group 8 Transition-Metal Complexes
36. Theoretical Study on Internal Alkyne/Vinylidene Isomerization in Group 8 Transition-Metal Complexes
Otsuka, M.; Tsuchida, N.; Ikeda, Y.; Lambert, N.; Nakamura, R.; Mutoh, Y.; Ishii, Y.; Takano, K.
Organometallics 2015, 34 (16), 3934–3943. DOI: 10.1021/om501280c
Ranked in the Top 20 Most downloaded Article for a Month
35. Synthesis of [3]Rotaxanes by the Combination of Copper-Mediated Coupling Reaction and Metal-Template Approach
35. Synthesis of [3]Rotaxanes by the Combination of Copper-Mediated Coupling Reaction and Metal-Template Approach
Hayashi, R.; Mutoh, Y.; Kasama, T.; Saito, S.
J. Org. Chem. 2015, 80 (15), 7536–7546. DOI: 10.1021/acs.joc.5b01120
34. A Macrocyclic Phenanthroline–Copper Complex with Less Steric Hindrance: Synthesis, Structure, and Application to the Synthesis of a [2]Rotaxane
34. A Macrocyclic Phenanthroline–Copper Complex with Less Steric Hindrance: Synthesis, Structure, and Application to the Synthesis of a [2]Rotaxane
Saito, S.; Ohkubo, T.; Yamazaki, Y.; Yokoyama, T.; Mutoh, Y.; Yamasaki, R.; Kasama, T.
Bull. Chem. Soc. Jpn. 2015, 88 (9), 1323–1330. DOI: 10.1246/bcsj.20150168
33. Synthesis of [3]Rotaxanes that Utilize the Catalytic Activity of a Macrocyclic Phenanthroline-Cu Complex: Remarkable Effect of the Length of the Axle Precursor
33. Synthesis of [3]Rotaxanes that Utilize the Catalytic Activity of a Macrocyclic Phenanthroline-Cu Complex: Remarkable Effect of the Length of the Axle Precursor
Yamashita, Y.; Mutoh, Y.; Yamasaki, R.; Kasama, T.; Saito, S.
Chem. - Eur. J. 2015, 21 (5), 2139–2145. DOI: 10.1002/chem.201405090
32. Synthesis of Rhodium−Primary Thioamide Complexes and Their Desulfurization Leading to Rhodium Sulfido Cubane-Type Clusters and Nitriles
32. Synthesis of Rhodium−Primary Thioamide Complexes and Their Desulfurization Leading to Rhodium Sulfido Cubane-Type Clusters and Nitriles
Mutoh, Y.; Sakigawara, M.; Niiyama, I.; Saito, S.; Ishii, Y.
Organometallics 2014, 33 (19), 5414–5422. DOI: 10.1021/om500714c
31. Acid-Mediated Ring-Expansion Reaction of N-Aryl-2-vinylazetidines: Synthesis and Unanticipated Reactivity of Tetrahydrobenzazocines.
31. Acid-Mediated Ring-Expansion Reaction of N-Aryl-2-vinylazetidines: Synthesis and Unanticipated Reactivity of Tetrahydrobenzazocines.
Shimizu, T.; Koya, S.; Yamasaki, R.; Mutoh, Y.; Azumaya, I.; Katagiri, K.; Saito, S.
J. Org. Chem. 2014, 79 (10), 4367–4377. DOI: 10.1021/jo500249c
30. Synthesis of Rotacatenanes by the Combination of Cu-Mediated Threading Reaction and the Template Method: The Dual Role of One Ligand
30. Synthesis of Rotacatenanes by the Combination of Cu-Mediated Threading Reaction and the Template Method: The Dual Role of One Ligand
Hayashi, R.; Wakatsuki, K.; Yamasaki, R.; Mutoh, Y.; Kasama, T.; Saito, S.
Chem. Commun. 2014, 50 (2), 204–206. DOI: 10.1039/C3CC47425A
29. A Redox-Active Porous Coordination Network Film Based on a Ru Complex as a Building Block on an ITO Electrode
29. A Redox-Active Porous Coordination Network Film Based on a Ru Complex as a Building Block on an ITO Electrode
Shinomiya, T.; Ozawa, H.; Mutoh, Y.; Haga, M.-A.
Dalton Trans. 2013, 42 (45), 16166–16175. DOI: 10.1039/c3dt51484f
This article is part of the themed collection: Coordination Programming: Science of Molecular Superstructures Towards Chemical Devices
28. Reactivities of Indenylruthenium Complex toward Internal Alkynes: Formation of Disubstituted Vinylidene Complexes and Indenyl−Alkyne Coupling
28. Reactivities of Indenylruthenium Complex toward Internal Alkynes: Formation of Disubstituted Vinylidene Complexes and Indenyl−Alkyne Coupling
Ikeda, Y.; Mutoh, Y.; Imai, K.; Tsuchida, N.; Takano, K.; Ishii, Y.
Organometallics 2013, 32 (15), 4353–4358. DOI: 10.1021/om4004913
27. Synthesis of [2]Rotaxanes by the Copper-Mediated Threading Reactions of Aryl Iodides with Alkynes
27. Synthesis of [2]Rotaxanes by the Copper-Mediated Threading Reactions of Aryl Iodides with Alkynes
Ugajin, K.; Takahashi, E.; Yamasaki, R.; Mutoh, Y.; Kasama, T.; Saito, S.
Org. Lett. 2013, 15 (11), 2684–2687. DOI: 10.1021/ol400992p
26. Synthesis of Monocyclic Nine-Membered Compounds by the [4+3+2] Cycloaddition-Bond Cleavage Strategy
26. Synthesis of Monocyclic Nine-Membered Compounds by the [4+3+2] Cycloaddition-Bond Cleavage Strategy
Yamasaki, R.; Kato, K.; Hanitani, D.; Mutoh, Y.; Saito, S.
Tetrahedron Lett. 2013, 54 (27), 3507–3509. DOI: 10.1016/j.tetlet.2013.04.094
25. Synthesis of Large [2]Rotaxanes. The Relationship between the Size of the Blocking Group and the Stability of the Rotaxane
25. Synthesis of Large [2]Rotaxanes. The Relationship between the Size of the Blocking Group and the Stability of the Rotaxane
Saito, S.; Takahashi, E.; Wakatsuki, K.; Inoue, K.; Orikasa, T.; Sakai, K.; Yamasaki, R.; Mutoh, Y.; Kasama, T.
J. Org. Chem. 2013, 78 (8), 3553–3560. DOI: 10.1021/jo302800t
24. Transformations of Alkynes at a Cyclotriphosphato Ruthenium Complex
24. Transformations of Alkynes at a Cyclotriphosphato Ruthenium Complex
Kanao, K.; Ikeda, Y.; Kimura, K.; Kamimura, S.; Tanabe, Y.; Mutoh, Y.; Iwasaki, M.; Ishii, Y.
Organometallics 2013, 32 (2), 527–537. DOI: 10.1021/om3009926
23. DFT Study of Internal Alkyne-to-Disubstituted Vinylidene Isomerization in [CpRu(PhC≡CAr)(dppe)]+
23. DFT Study of Internal Alkyne-to-Disubstituted Vinylidene Isomerization in [CpRu(PhC≡CAr)(dppe)]+
Otsuka, M.; Tsuchida, N.; Ikeda, Y.; Kimura, Y.; Mutoh, Y.; Ishii, Y.; Takano, K.
J. Am. Chem. Soc. 2012, 134 (42), 17746–17756. DOI: 10.1021/ja308018b
22. Formation of (Alkenylphosphonio)phenylruthenium Complexes from Diphenylacetylene and a [CpRu(dppm)] Cation: Experimental Evidence for the Equilibrium between η1-Disubstituted Vinylidene and η2-Internal Alkyne
22. Formation of (Alkenylphosphonio)phenylruthenium Complexes from Diphenylacetylene and a [CpRu(dppm)] Cation: Experimental Evidence for the Equilibrium between η1-Disubstituted Vinylidene and η2-Internal Alkyne
Mutoh, Y.; Kimura, Y.; Ikeda, Y.; Tsuchida, N.; Takano, K.; Ishii, Y.
Organometallics 2012, 31 (14), 5150–5158. DOI: 10.1021/om3004948
21. Synthesis and Skeletal Transformation of Cyanamido(2−)- and Cyanamido(1−)-Bridged Ruthenium Complexes with Hexamethylbenzene Ligands
21. Synthesis and Skeletal Transformation of Cyanamido(2−)- and Cyanamido(1−)-Bridged Ruthenium Complexes with Hexamethylbenzene Ligands
Nogami, T.; Imaji, M.; Uemura, K.; Tanabe, Y.; Mutoh, Y.; Ishii, Y.
Chem. Lett. 2011, 40 (10), 1167–1169. DOI: 10.1246/cl.2011.1167
20. Conformational Change of Ternary Copper(II) Complexes of Cationic Schiff-Bases and N-Heteroaromatic Amines Induced by Intercalative Binding to DNA
20. Conformational Change of Ternary Copper(II) Complexes of Cationic Schiff-Bases and N-Heteroaromatic Amines Induced by Intercalative Binding to DNA
Iwasaki, Y.; Kimura, M.; Yamada, A.; Mutoh, Y.; Tateishi, M.; Arii, H.; Kitamura, Y.; Chikira, M.
Inorg. Chem. Commun. 2011, 14 (9), 1461–1464. DOI: 10.1016/j.inoche.2011.05.047
19. Reversibility of Disubstituted Vinylidene−Internal Alkyne Isomerization at Cationic Ruthenium and Iron Complexes
19. Reversibility of Disubstituted Vinylidene−Internal Alkyne Isomerization at Cationic Ruthenium and Iron Complexes
Mutoh, Y.; Imai, K.; Kimura, Y.; Ikeda, Y.; Ishii, Y.
Organometallics 2011, 30 (2), 204–207 (Communication). DOI: 10.1021/om101109c
Ranked in the Top 20 Most downloaded Article for a Month
18. Ruthenium Seleno- and Tellurocarbonyl Complexes: Selenium and Tellurium Atom Transfer to a Terminal Carbido Ligand
18. Ruthenium Seleno- and Tellurocarbonyl Complexes: Selenium and Tellurium Atom Transfer to a Terminal Carbido Ligand
Mutoh, Y.; Kozono, N.; Araki, M.; Tsuchida, N.; Takano, K.; Ishii, Y.
Organometallics 2010, 29 (3), 519–522 (Communication). DOI: 10.1021/om901029w
17. The Effects of Primary Structures on Photo-Induced Insolubilization of All-Cis Poly(p-phenylenevinylene)s in Thin Films
17. The Effects of Primary Structures on Photo-Induced Insolubilization of All-Cis Poly(p-phenylenevinylene)s in Thin Films
Mutoh, Y.; Yamamoto, Y.; Wakioka, M.; Takita, R.; Nakamura, J.; Iida, T.; Ozawa, F.
Bull. Chem. Soc. Jpn. 2009, 82 (12), 1533–1537. DOI: 10.1246/bcsj.82.1533
16. A Highly Selective Catalytic System for the Cross-Coupling of (E)-Styryl Bromide with Benzeneboronic Acid: Application to the Synthesis of All-Trans Poly(arylenevinylene)s
16. A Highly Selective Catalytic System for the Cross-Coupling of (E)-Styryl Bromide with Benzeneboronic Acid: Application to the Synthesis of All-Trans Poly(arylenevinylene)s
Wakioka, M.; Mutoh, Y.; Takita, R.; Ozawa, F.
Bull. Chem. Soc. Jpn. 2009, 82 (10), 1292–1298. DOI: 10.1246/bcsj.82.1292
Highlighted as a Selected Paper
15. Syntheses and Stability of Alkynyl S,N-Acetals Derived from 2-Propynals
15. Syntheses and Stability of Alkynyl S,N-Acetals Derived from 2-Propynals
Murai, T.; Fukushima, K.; Ohta, Y.; Mutoh, Y.
Phosphorus, Sulfur Silicon Relat. Elem. 2009, 184 (6), 1462–1480. DOI: 10.1080/104265009029 47765
Part of the Special Issue: Honoring the 70th Birthday of Marian Mikolajczyk
14. Internal Alkyne-to-vinylidene Isomerization at Cationic Ruthenium and Iron Complexes
14. Internal Alkyne-to-vinylidene Isomerization at Cationic Ruthenium and Iron Complexes
Mutoh, Y.; Ikeda, Y.; Kimura, Y.; Ishii, Y.
Chem. Lett. 2009, 38 (6), 534–535. DOI: 10.1246/cl.2009.534
13. Core Expansion Reactions of Cyanamido/Carbodiimido-Bridged Polynuclear Iridium Complexes
13. Core Expansion Reactions of Cyanamido/Carbodiimido-Bridged Polynuclear Iridium Complexes
Imaji, M.; Tanabe, Y.; Mutoh, Y.; Ishii, Y.
Inorg. Chem. 2009, 48 (2), 773–780. DOI: 10.1021/ic8017503
12. Formation of Vinylidenes from Internal Alkynes at a Cyclotriphosphato Ruthenium Complex
12. Formation of Vinylidenes from Internal Alkynes at a Cyclotriphosphato Ruthenium Complex
Ikeda, Y.; Yamaguchi, T.; Kanao, K.; Kimura, K.; Kamimura, S.; Mutoh, Y.; Tanabe, Y.; Ishii, Y.
J. Am. Chem. Soc. 2008, 130 (50), 16856–16857 (Communication). DOI: 10.1021/ja8080567
11. Synthesis and Properties of 1-Methylthiopropargylammonium Salts and Their Use as Key Precursors to Sulfur-Containing Enediynes
11. Synthesis and Properties of 1-Methylthiopropargylammonium Salts and Their Use as Key Precursors to Sulfur-Containing Enediynes
Murai, T.; Fukushima, K.; Mutoh, Y.
Org. Lett. 2007, 9 (25), 5295–5298. DOI: 10.1021/ol7024923
10. Sequential Addition Reactions of Lithium Acetylides and Grignard Reagents to Selenoiminium Salts Leading to 2-Propynyl Tertiary Amines Bearing a Tetrasubstituted Carbon Center
10. Sequential Addition Reactions of Lithium Acetylides and Grignard Reagents to Selenoiminium Salts Leading to 2-Propynyl Tertiary Amines Bearing a Tetrasubstituted Carbon Center
Murai, T.; Nogawa, S.; Mutoh, Y.
Bull. Chem. Soc. Jpn. 2007, 80 (11), 2220–2225. DOI: 10.1246/bcsj.80.2220
Highlighted as a Selected Paper
9. Telluration of Seleno- and Chloroiminium Dalts Leading to Various Telluroamides, and Their Structure and NMR Properties
9. Telluration of Seleno- and Chloroiminium Dalts Leading to Various Telluroamides, and Their Structure and NMR Properties
Mutoh, Y.; Murai, T.; Yamago, S.
J. Organomet. Chem. 2007, 692 (1–3), 129–135. DOI: 10.1016/j.jorganchem.2006.03.045
Part of the Special issue for "Reaction Control in Dynamic Complexes"
8. Sequential Addition Reaction of Lithium Acetylides and Grignard Reagents to Thioiminium Salts from Thiolactams Leading to 2,2-Disubstituted Cyclic Amines
8. Sequential Addition Reaction of Lithium Acetylides and Grignard Reagents to Thioiminium Salts from Thiolactams Leading to 2,2-Disubstituted Cyclic Amines
Murai, T.; Toshio, R.; Mutoh, Y.
Tetrahedron 2006, 62 (26), 6312–6320. DOI: 10.1016/j.tet.2006.04.065
7. Substituent Effects on [1,3]-Rearrangement of Alkynyl S,N-Acetals to 1-Amino-3-Sulfenylallenes and their Conversion to α,β-Unsaturated Ketones
7. Substituent Effects on [1,3]-Rearrangement of Alkynyl S,N-Acetals to 1-Amino-3-Sulfenylallenes and their Conversion to α,β-Unsaturated Ketones
Murai, T.; Mutoh, Y.; Fukushima, K.
Lett. Org. Chem. 2006, 3 (5), 409–413. DOI: 10.2174/157017806776611872
6. Addition Reaction of Zinc Acetylides to Thioiminium Salts Leading to 3-Amino-1-Sulfenyl-1,4-Enynes
6. Addition Reaction of Zinc Acetylides to Thioiminium Salts Leading to 3-Amino-1-Sulfenyl-1,4-Enynes
Murai, T.; Ohta, Y.; Mutoh, Y.
Tetrahedron Lett. 2005, 46 (21), 3637–3640. DOI: 10.1016/j.tetlet.2005.03.166
5. Acyclic Telluroiminium Salts: Isolation and Characterization
5. Acyclic Telluroiminium Salts: Isolation and Characterization
Mutoh, Y.; Murai, T.; Yamago, S.
J. Am. Chem. Soc. 2004, 126 (51), 16696–16697 (Communication). DOI: 10.1021/ja044022n
4. Synthesis and Properties of Selenoiminium Salts Derived from Secondary Selenoamides
4. Synthesis and Properties of Selenoiminium Salts Derived from Secondary Selenoamides
Mutoh, Y.; Murai, T.
Organometallics 2004, 23 (16), 3907–3913. DOI: 10.1021/om0497339
3. Synthesis of Tertiary Propargylamines by Sequential Reactions of in Situ Generated Thioiminium Salts with Organolithium and -Magnesium Reagents
3. Synthesis of Tertiary Propargylamines by Sequential Reactions of in Situ Generated Thioiminium Salts with Organolithium and -Magnesium Reagents
Murai, T.; Mutoh, Y.; Ohta, Y.; Murakami, M.
J. Am. Chem. Soc. 2004, 126 (19), 5968–5969 (Communication). DOI: 10.1021/ja048627v
2. Acyclic Selenoiminium Salts: Isolation, First Structural Characterization, and Reactions
2. Acyclic Selenoiminium Salts: Isolation, First Structural Characterization, and Reactions
Mutoh, Y.; Murai, T.
Org. Lett. 2003, 5 (8), 1361–1364. DOI: 10.1021/ol034334f
1. MeOTf-Mediated Alkynylation of Selenoamides Leading to β-Methylselenenyl α,β-Unsaturated Ketones and Their Characterization
1. MeOTf-Mediated Alkynylation of Selenoamides Leading to β-Methylselenenyl α,β-Unsaturated Ketones and Their Characterization
Murai, T.; Mutoh, Y.; Kato, S.
Org. Lett. 2001, 3 (13), 1993–1995. DOI: 10.1021/ol015968u
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