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Publications & Patents

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Original Publications

2024

46. Y. Hisata, T. Washio, S. Takizawa, S. Ogoshi, Y. Hoshimoto,* “In-Silico-Assisted Derivatization of Triarylboranes for the Catalytic Reductive Functionalization of Amino Acids with H2,” submitted.

ChemRxiv 2023, preprint (DOI: 10.26434/chemrxiv-2023-3mwbd). 

45. Y. Yamauchi, S. Ogoshi, Y. Uetake,* Y. Hoshimoto,* “Reversible Modulation of the Local Environment around Metal Centers Bearing Multifunctional Carbenes,” Chem. Lett. 2024, 53, upae042. OPEN ACCESS; Highlighted Review

44. J.N. Leung, Y. Mondori, S. Ogoshi, Y. Hoshimoto,* H. V. Huynh,* “Electronic Profiling of N-Phosphie Oxide-Substituted Imidazolin-2-ylidenes (PoxIms) and Imidazolidin-2-ylidenes (SPoxIms),” Inorg. Chem. 2024, 63, 4344-4354.

43. S. Manna, F. Papp, Y. Hisata, J. Löffler, M. Rybka, V.H. Gessner,* Y. Hoshimoto,* L. J. Gooßen,* “Palladium-Catalyzed γ-Arylation of Acylketene Synthons with Aryl Chlorides Enabled by Ylide-Functionalized Phosphines (YPhos),” Adv. Synth. Catal. 2024, 366, 1107-1112. OPEN ACCESS; Very Important Publication (VIP)

42. M. Sakuraba, S. Ogoshi, Y. Hoshimoto,* “Strategic Use of Crude H2 for the Catalytic Reduction of Carbonyl Compounds,” Tetrahedron Chem, 2024, 9, 100059. OPEN ACCESS; Special issue “Organocatalysis”

2023

41. M. Sakuraba, T. Morishita, T. Hashimoto, S. Ogoshi,* Y. Hoshimoto,* “Remote Back Strain: A Strategy for Modulating the Reactivity of Triarylboranes,” Synlett, 2023, 34, 2187-2192. Special issue “Modern Boron Chemistry: 60 years of the Matteson Reaction

40. Y. Yamauchi, Y. Mondori, Y. Uetake,* Y. Takeichi, T. Kawakita, H. Sakurai, S. Ogoshi,* Y. Hoshimoto,* “Reversible Modulation of the Electronic and Spatial Environment around Ni(0) Centers Bearing Multifunctional Carbene Ligands with Triarylaluminum,” J. Am. Chem. Soc. 2023, 145, 16938-16947. OPEN ACCESS.

ChemRxiv 2023, preprint (DOI: 10.26434/chemrxiv-2023-5nz52). 

39. S. Nagai, T. Hinogami, S. Ogoshi,* Y. Hoshimoto,* “N-Borane-Substituted Cyclic Phosphine Imides (BCPIS),” Bull. Chem. Soc. Jpn. 2023, 96, 1346-1353. OPEN ACCESS; Selected Paper; Inside Cover.

ChemRxiv 2023, preprint (DOI: 10.26434/chemrxiv-2023-qv422-v2). 

2022

38. Y. Hoshimoto,* Y. Yamauchi, T. Tomoya, S. Ogoshi, “Complexation-Induced N‒P Axial Chirality in Sm(II) N-Phosphine-Oxide-Substituted Imidazolylidene and Imidazolinylidene Complexes,” Can. J. Chem. 2022, 101, 429-433. Special issue in “Honour of Cathleen Crudden

ChemRxiv 2022, preprint (DOI: 10.26434/chemrxiv-2022-rf1wd). 

37. T. Hashimoto, T. Asada, S. Ogoshi,* Y. Hoshimoto,* “Main group catalysis for H2 purification based on liquid organic hydrogen carriers,” Science Adv. 2022, 8,  eade0189. OPEN ACCESS. PRESS Release (Japanese). Featured by EurekAlert; AlphaGalileo, Asia Research News; PhysOrg; Scienmag; Nanowerk; AZo Materials; 時事通信ニュース; YAHOO!; Cosmos Magazine; MIT Tech Review; 日経xTech; Chem-Station; 現代化学2023年1月号; クリーンエネルギー2023年4月号(Vol.32, 54-61; 日本工業出版) ; New Energy and Fuel

ChemRxiv 2022, preprint (DOI: 10.26434/chemrxiv-2022-pgbgd).

36. Y. Yamauchi, Y. Hoshimoto,* T. Kawakita, T. Kinoshita, Y. Uetake, H. Sakurai, S. Ogoshi,* “Room-Temperature Reversible Chemisorption of Carbon Monoxide on Nickel(0) Complexes,” J. Am. Chem. Soc. 2022, 144, 8818-8826. OPEN ACCESS. Press Release (Japanese), 現代化学2022年7月号, Chem-Station.

ChemRxiv 2022, preprint (DOI: 10.26434/chemrxiv-2022-nb0fw);

2021

35. Y. Hoshimoto,* M. Sakuraba, T. Kinoshita, M. Ohbo, M. Ratanasak, J. Hasegawa,* S. Ogoshi,* “A boron-transfer mechanism mediating the thermally induced revival of frustrated carbene−borane pairs from their shelf-stable adducts,” Commun. Chem. 2021, 4, 137. OPEN ACCESS

ChemRxiv 2021, preprint (DOI: 10.26434/chemrxiv.14462391.v1).

34. Y. Yamauchi, S. Nagai, T. Terada, Y. Hoshimoto,* S. Ogoshi,* “Sm(II)-Mediated Single-Electron Reduction of Pentafluorophenylcopper(I),” Chem. Lett. 2021, 50, 1394-1396. These authors equally contributed to this work. OPEN ACCESS

33. Y. Hoshimoto,* S. Nagai, T. Hinogami, S. Hazra, S. Ogoshi,* “N‐Phosphine Imide‐Substituted Imidazolylidenes (PimIms),” Asian J. Org. Chem. 2021, 10, 1085-1089. Special issue “Early Career Special Collection“.

32. Y. Hoshimoto,* S. Ogoshi,* “Development of Metal Complexes Equipped with Structurally Flexible Carbenes,”Bull. Chem. Soc. Jpn. 2021, 94, 327-338. OPEN ACCESS; Inside Cover; Award Account for The 67th Chemical Society of Japan Award for Young Chemists (第67回進歩賞受賞論文).

2020

31. K. Asida, Y. Hoshimoto, S. Ogoshi,* “Ni(0)-Catalyzed Synthesis of Polycyclic α,β-Unsaturated γ-Lactams via Intramolecular Carbonylative Cycloaddition of Yne-imines with CO, Synlett 2021, 32, 1537-1541.

30. T. Asada, Y. Hoshimoto,* S. Ogoshi,* “Rotation-Triggered Transmetalation on Heterobimetallic Cu/Al N-Phosphine-Oxide-Substituted Imidazolylidene Complex, J. Am. Chem. Soc. 2020, 142, 9772-9784. OPEN ACCESS.

29. T. Asada, Y. Hoshimoto,* T. Kawakita, T. Kinoshita, S. Ogoshi,* “Axial Chirality around N‒P Bonds Induced by Complexation between E(C6F5)3 (E = B, Al) and an N-Phosphine-Oxide-Substituted Imidazolinylidene: A Key Intermediate in the Catalytic Phosphinoylation of CO2, J. Org. Chem. 2020,85, 14333-14341 . Special issue “The New Golden Age of Organophosphorus Chemistry“. OPEN ACCESS. One of the Most Read Articles.

28. K. Ashida, Y. Hoshimoto, N. Tohnai, D. E. Scott, M. Ohashi, H. Imaizumi, Y. Tsuchiya, S. Ogoshi,*  “Enantioselective Synthesis of Polycyclic γ-Lactams with Multiple Chiral Carbon Centers via Ni(0)-Catalyzed Asymmetric Carbonylative Cycloadditions without Stirring,” J. Am. Chem. Soc. 2020, 142, 1594-1602.

27. Y. Hoshimoto, C. Nishimura, Y. Sasaoka, R. Kumar, S. Ogoshi,*  “Catalytic Synthesis of Isoquinolines via Intramolecular Migration of N-Aryl Sulfonyl Groups on 1,5-Yne-Imines,” Bull. Chem. Soc. Jpn. 2020, 93, 182-186. OPEN ACCESS

2019

26. Y. Hoshimoto,* S. Ogoshi,* “Triarylborane-Catalyzed Reductive N-Alkylation of Amines: A Perspective,” ACS Catal. 2019, 9, 5439.

25. T. Kinoshita, M. Sakuraba, Y. Hoshimoto,* S. Ogoshi,* “Complexation between MTOf (M = Li and Na) and N-Phosphine oxide-substituted Imidazolylidenes via Coordination of the N-Phosphoryl Groups,” Chem. Lett. 2019, 48, 230. OPEN ACCESS

2018

24. Y. Hoshimoto,* T. Kinoshita, S. Hazra, M. Ohashi, S. Ogoshi,* “Main-Group-Catalyzed Reductive Alkylation of Multiply Substituted Amines with Aldehydes Using H2,J. Am. Chem. Soc. 2018, 140, 7292. PRESS RELEASE (JP). EurekAlert. AlphaGalileo. 日経バイオテクONLINE(JP). PhysOrg. SienceDaily. 化学工業 (CHEMICAL INDUSTRY, 2018, 69, 551-552). academist Journal (2018.7.9).

2017

23. S. Hazra, Y. Hoshimoto,* S. Ogoshi,* “N-Phosphine Oxide-Substituted Imidazolylidenes (PoxIms): Multifunctional Multipurpose Carbenes,Chem. Eur. J. 2017, 23, 15238. Invited ‘Concept’ article; OPEN ACCESS; Most Accessed article on 2017 (from Oct. to Dec.).

22. Y. Hoshimoto,* T. Asada, S. Hazra, M. Ohashi, S. Ogoshi,* “Phosphorylation of Isocyanates and Aldehydes by Multifunctional N-Phosphine Oxide-Substituted Imidazolylidenes,Chem. Lett. 2017, 46, 1211. OPEN ACCESS

21. Y. Hayashi, Y. Hoshimoto, R. Kumar, M. Ohashi, S. Ogoshi,* “Nickel(0)-Catalyzed Coupling Reactions of Carbonyls and Alkenes with Reducing Reagents Giving Six- and Seven-Membered Benzocycloalkanols,” Chem. Lett. 2017, 46, 1096. OPEN ACCESS

20. Y. Hoshimoto, K. Ashida, Y. Sasaoka, R. Kumar, K. Kamikawa, X. Verdaguer, A. Riera, M. Ohashi, S. Ogoshi,* “Efficient Synthesis of Polycyclic g-Lactams by Catalytic Carbonylation of Ene-Imines via Nickelacycle Intermediate,” Angew. Chem. Int. Ed. 2017, 56, 8206.

19. K. Ravindra, Y. Hoshimoto, E. Tamai, M. Ohashi, S. Ogoshi,* “Two-step synthesis of chiral fused tricyclic scaffolds from phenols via desymmetrization on nickel,” Nature Commun. 2017, 8, 32. OPEN ACCESS

18. W. Tao, S. Akita, R. Nakano, S. Ito, Y. Hoshimoto, S. Ogoshi, K. Nozaki,* “Copolymerisation of ethylene with polar monomers by using palladium catalysts bearing an N-heterocyclic carbene-phosphine oxide bidentate ligand,” Chem. Commun. 2017, 53, 2630-2633.

17. Y. Hoshimoto, Y. Hayashi, M. Ohashi, and S. Ogoshi,* “Kinetic and Theoretical Studies on Ni(0)/N-Heterocyclic Carbene-Catalyzed Intramolecular Alkene Hydroacylation,” Chem. Asian J. 2017, 12, 278-282.

2016

16. Y. Hoshimoto,* T. Asada, S. Hazra, T. Kinoshita, P. Sombut, R. Kumar, M. Ohashi, S. Ogoshi,* “Strategic Utilization of Multifunctional Carbene for Direct Synthesis of Carboxylic-Phosphinic Mixed Anhydride from CO2,Angew. Chem. Int. Ed. 2016, 55, 16075-16079. OPEN ACCESS

15. R. Kumar, E. Tamai, A. Ohnish, A. Nishimura, Y. Hoshimoto, M. Ohashi, and S. Ogoshi,* “Nickel-Catalyzed Enantioselective Synthesis of Cyclobutenes via [2+2] Cycloaddition of a,b-Unsaturated Carbonyls with 1,3-Enynes,” Synthesis 2016, 48, 2789-2794.

14. Y. Hayashi, Y. Hoshimoto, R. Kumar, M. Ohashi, S. Ogoshi,* “Nickel(0)-catalyzed intramolecular reductive coupling of alkenes and aldehydes or ketones with hydrosilanes,” Chem. Commun. 2016, 6237-6240. OPEN ACCESS

13. R. Kumar, H. Tokura, A. Nishimura, T. Mori, Y. Hoshimotoi, M. Ohashi, and S. Ogoshi,* “Nickel(0)/N-Heterocyclic Carbene-Catalyzed Asymmetric [2+2+2] Cycloaddition of Two Enones and an Alkyne: Access to Cyclohexenes with Four Contiguous Stereogenic Centers,” Org. Lett. 2015, 17, 6018-6021.

2015

12. R. Kumar, Y. Hoshimoto, H. Yabuki, M. Ohashi, S. Ogoshi,* “Nickel(0)-Catalyzed Enantio- and Diastereoselective Synthesis of Benzoxasiloles: Ligand-Controlled Switching from Inter- to Intramolecular Aryl-Transfer Process,” J. Am. Chem. Soc. 2015, 137, 11838-11845.

11. Y. Hoshimoto,* T. Kinoshita, M. Ohashi, S. Ogoshi,* “A Strategy to Control the Reactivation of Frustrated Lewis Pairs from Shelf-Stable Carbene-Borane Complexes,” Angew. Chem. Int. Ed. 2015, 54, 11666-11671. OPEN ACCESS; Highlighted in a Front Cover, and Altals of Science, November 18th, 2015: “Control the frustration between molecular pairs with external stimuli-responsive motions,” and Chemistry Today (Tokyo Kagaku Doujin Co.), March 2016.

10. Y. Kita, H. Sakaguchi, Y. Hoshimoto, D. Nakauchi, Y. Nakahara, J.-F. Carpentier, S. Ogoshi, K. Mashima,* “Pentacoordinated Carboxylate π-Allyl Nickel Complexes as Key Intermediates for Ni-catalyzed Direct Amination of Allylic Alcohols,” Chem. Eur. J. 2015, 21, 14571-14578.

9. Y. Hoshimoto, M. Ohashi, S. Ogoshi,* “Catalytic Transformation of Aldehydes with Nickel Complexes through η2 Coordination and Oxidative Cyclization,” Acc. Chem. Res. 2015, 48, 1746-1755. Account Special Issue for “Earth Abundant Metals in Homogeneous Catalysis”

8. M. Ohashi, Y. Hoshimoto, S. Ogoshi,* “Aza-Nickelacycle Key Intermediate in Nickel(0)-Catalyzed Transformation Reactions,” Dalton Trans. 2015, 44, 12060-12073. Perspective

2014

7. Y. Hoshimoto, H. Yabuki, R. Kumar, H. Suzuki, M. Ohashi, S. Ogoshi,* “Highly Efficient Activation of Organosilanes with η2-Aldehyde Nickel Complexes: Key for Catalytic Syntheses of Aryl-, Vinyl-, and Alkynyl-benzoxasiloles,” J. Am. Chem. Soc. 2014, 136, 16752-16755.

6. Y. Hoshimoto, T. Ohata, Y. Sasaoka, M. Ohashi, S. Ogoshi,* “Nickel(0)-Catalyzed [2+2+1] Carbonylative Cycloaddition of Imines and Alkynes or Norbornene Leading to g-Lactams,” J. Am. Chem. Soc. 2014, 136, 15877-15880. Highlighted in C&E NEWS 2014, 92, 35.

5. Y. Hoshimoto, Y. Hayashi, H. Suzuki, M. Ohashi, S. Ogoshi,* “One-Pot, Single-Step and Gram-Scale Synthesis of Mononuclear [(η6-arene)Ni(N-heterocyclic Carbene)] Complexes; Useful Precursors of the Ni0-NHC Unit,” Organometallics 2014, 33, 1276-1282. Selected as one of the top 20 downloaded articles.

4. Y. Hoshimoto, T. Ohata, M. Ohashi, S. Ogoshi,* “Nickel-Catalyzed Synthesis of N-Aryl-1,2-Dihydropyridines by [2+2+2] Cycloaddition of Imines with Alkynes via T-Shaped 14-Electron Aza-Nickelacycle Key Intermediates,” Chem. Eur. J. 2014, 20, 4105-4110.

2012

3. Y. Hoshimoto, Y. Hayashi, H. Suzuki, M. Ohashi, S. Ogoshi,* “Synthesis of Five- and Six-Membered Benzocyclic Ketones through Intramolecular Alkene Hydroacylation Catalyzed by Nickel(0)/N-Heterocyclic Carbenes,” Angew. Chem. Int. Ed. 2012, 51, 10812-10815.

2011

2. Y. Hoshimoto, M. Ohashi, S. Ogoshi,* “Nickel-Catalyzed Selective Conversion of Two Different Aldehydes to Cross-Coupled Esters,” J. Am. Chem. Soc. 2011, 133, 4668-4671. Selected as Most Read Articles (1st place) on May, 2011; Highlighted in Angew. Chem. Int. Ed. 2011, 50, 11047-11049, and Kagaku, 2011, 9, 12-16.

2010

1. S. Ogoshi,* Y. Hoshimoto, M. Ohashi, “Nickel-catalyzed Tishchenko reaction via hetero-nickelacycles by oxidative cyclization of aldehydes with nickel(0) complex,” Chem. Commun. 2010, 46, 3354-3356.

Original Patents (Applications)

P5. Y. Hoshimoto, “Boron compound, and preparation of hydrogenated compound and polymer thereby”, Application No. JP2023-95773; Application Date: 2023-06-09.

P4. Y. Hoshimoto, S. Ogoshi, “Boron compound, and preparation of hydrogenated compound and polymer thereby”, Application No. JP2022-195051 (Application Date: 2022-12-06); Application No. JP2023-185532 (Application Date: 2023-10-30)

P3. Y. Hoshimoto, S. Ogoshi, T. Kawamoto, T. Tanaka, “Boron compound, and preparation of hydrogenated compound and polymer thereby”, JP7079696 (Publication Date: 2022-06-02; Application No. JP2018-160332; Application Date: 2018-08-29)

P2. Y. Hoshimoto, S. Ogoshi, T. Tomoaki, T. Kawamoto, “Method for hydrogenation of unsaturated compounds using crude hydrogen and frustrated Lewis pair”, JP2017206474A (Publication Date: 2017-11-24; Application No. JP2016-100976; Application Date: 2016-05-20).

P1. Y. Hoshimoto, S. Ogoshi, T. Kawamoto, JP6569973 (Publication Date: 2019-8-16; Application No. JP2014-206649; Application Date: 2014-10-7).

Other Contributions

⁂8. 橋本 大樹, 星本 陽一,* 粗水素から水素を抜き出す世界初の分子技術,” クリーンエネルギー (技術情報協会), 2023, Vol. 32, No. 4, 54-62.

⁂7. 橋本 大樹, 星本 陽一,* 典型元素化合物を用いた粗水素条件下における触媒的水素化反応ー有機ハイドライドを水素精製へ活用する技術基盤ー,” [水素の製造とその輸送, 貯蔵, 利用技術], 第3章9節, 技術情報協会.

⁂6. 山内 泰宏, 星本 陽一,* 生越 專介,* “多用途な多官能基化環状カルベンPoxImの開発,” 有機合成化学協会誌, 2021, 79, 632-641. (in Japanese; 総合論文)

⁂5. Y. Hoshimoto,* “Transformation of Aldehydes via Nickelacycles” in Nickel Catalysis in Organic Synthesis: Methos and Reactions, Ed by S. Ogoshi, Wiley-VCH: Germany, 2020. (Book Chapter)

⁂4. 星本陽一, “典型元素触媒と水素を活用したクリーンなアミン変換法を実現!,” academist Journal, 2018年7月9日掲載.

⁂3. 星本陽一, “多機能・多用途カルベンの開発と応用,” 化学工業 (CHEMICAL INDUSTRY), 2018, 69, 477-481. (特集/イノベーションに挑戦する若手研究者) 

⁂2. 星本陽一, “2,2-ジアミノエノールを視る!N-ヘテロ環状カルベンによるアルデヒドの極性転換,” 有機合成化学協会誌 Review de Debut, 2014, 72, 1158-1159.

⁂1. 星本陽一, 大橋理人, 生越専介, “ついに攻略!!難攻不落の交差Tishchenko反応 Ni(0)を触媒とするアルデヒドの交差エステル合成,” 月刊 化学, 2011, 66, 12-16.

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