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Ryo murakami

  1. CO2分離改修貯留及び有効利用技術〜脱炭素社会での企業対応/CCS・CCUS/排出量計算
    稲垣冬彦,村上遼
    第3章第3節第10項
    株式会社情報機構
     

  2. Copper Complex Featuring Cation-Excess Alternation Counterion Catalyzing Mukaiyama-Aldol Reaction of Ketene Silyl Acetals and Ketones
    Tanishima, H.; Murakami, R.; Inagaki, F.
    Tetrahedron Lett. 2022, 100, 153885.
    DOI: org/10.1016/j.tetlet.2022.153885


  3. フェニル基を活用した選択的にCO2を吸収する吸収剤の開発
    稲垣冬彦, 村上 遼
    CO2の分離・回収・貯留の最新技術, NTS, 第2章-第4編-3
    https://books.rakuten.co.jp/rb/17106305/
     

  4. 二酸化炭素の発生方法 
    稲垣冬彦, 村上 遼, 大塚 里彩, 内田 彩花
    特願2022-020715
     

  5. 大気中水分を吸収しない革新的CO2選択的吸収・放出剤
    稲垣冬彦, 村上 遼
    化学工業 2021, 72, 9, 609-613.
     

  6. Diastereoselective Tricyclization/Dimerization of Yne-Indoles Catalyzed by a Au(III) Complex Featuring an L2/Z-Type Ligand
    Murakami, R.; Tanishima, H.; Naito, D.; Kawamitsu, H.; Kamo, R.; Uchida, A.; Kawasaki, K.; Kiyohara, C.; Matsuo, M.; Maeda, K.; Inagaki, F.
    Tetrahedron Lett. 2021, 78, 153267.
    DOI: 10.1016/j.tetlet.2021.153267

     

  7. Construction of 2,2-Dimethyloxepane Frameworks from Ene-Diols Catalyzed by Metal Catalyst or Brønsted Acid via 7-Endo-Trig Cyclization
    Murakami, R.; Maeda, K.; Inagaki, F.
    Chem. Pharm. Bull. 2021, 69, 892-895.
    DOI: org/10.1248/cpb.c21-00400

     

  8. 大気由来の二酸化炭素の吸収剤
    稲垣冬彦, 村上 遼, 川満 日香梨
    特願2021-026634
     

  9. Development of Gold-catalyzed Reaction Utilizing Electron Acceptability of Z-type Ligand
    Murakami, R.; Inagaki, F.
    YAKUGAKU ZASSHI 2021141, 305-314.
    DOI: 10.1248/yakushi.20-00179-1

     

  10. Z型配位子に特徴を有する金(I)錯体の合成とその触媒反応
    村上 遼, 稲垣 冬彦
    有機合成化学協会誌 2020, 78, 619-626. 
     

  11. Aliphatic Oxaboroles Enabling Remarkable Recognition of Diols
    Arakawa, N.; Nagao, K.; Murakami, R.; Sumida, Y.; Arakawa, H.; Inagaki, F.; Ohmiya, H.
    Bull. Chem. Soc. Jpn. 2020​,
    93, 576.
    DOI: 10.1246/bcsj.20200007​
    *Selected Paper
     

  12. Recent Topics of Gold Catalyst Featuring Z-Type Ligands
    Murakami, R.; Inagaki, F.
    Tetrahedron Lett.  2019,
     60, 151038.
    DOI: 10.1016/j.tetlet.2019.151038
     *Picked up by Org. Chem. Highlights
     https://www.organic-chemistry.org/Highlights/2020/11May.shtm
     

  13. Meta-xylylenediamine (MXDA)
    Murakami, R.; Inagaki, F. 
    Encyclopedia of Reagents for Organic Synthesis 2019
    DOI: 10.1002/047084289X.rn02285

     

  14. Coinage Metal Catalyzed 7-Endo-Trig Cyclization of Ene-Dios: Construction of 2,2-Dimethyloxepane Frameworks
    Maeda, K.; Murakami, R.; Inagaki, F.
    Tetrahedron Lett.  2019, 60, 151231.
    DOI: 10.1016/j.tetlet.2019.151231
     

  15. Control of site selectivity in trifluoromethylation of alkenes bearing a pendant indolyl group: Synthesis of CF3-containing tetrahedrocarbazoles
    Murakami, R.; Sekine, D.; Aoki, Y.; Kawamura, S.; Sodeoka, M.
    Tetrahedron 2019, 75, 1327-1335. 
    DOI: 10.1016/j.tet.2019.01.048

     

  16. Palladium-Catalyzed Asymmetric C(sp3)–H Allylation of 2-Alkylpyridines
    Murakami, R.; Sano, K.; Iwai, T.; Sawamura, M.
    Angew. Chem. Int. Ed. 2018, 57, 9465–9469.
    DOI: 10.1002/anie.201802821

     

  17. Site-selective and Stereoselective C(sp3)–H Borylation of Alkyl Side Chains of 1,3-Azoles with a Silica-Supported Monophosphine-Ir Catalyst
    Murakami, R.; Iwai, T.; Sawamura, M.
    Synlett. 2016, 27, 1187-1192. 
    DOI: 10.1055/s-0035-1561599

     

  18. Stereoselective C–H Borylations of Cyclopropanes and Cyclobutanes with Silica-supported Monophosphane-Ir Catalysts.
    Murakami, R.; Tsunoda,K.; Iwai, T.; Sawamura, M.
    Chem. Eur. J. 2014, 20, 13127–13131.
    DOI: 10.1002/chem.201404362

     

  19. Silica-Supported Tripod Triarylphosphane: Application to Transition Metal Catalyzed C(sp3)–H Borylations. 
    Iwai, T.; Murakami, R.; Harada,T.; Kawamorita, S.; Sawamura, M.
    Adv. Synth. Catal. 2014356, 1563–1570.
    DOI: 10.1002/adsc.201301147

     

  20. Synthesis of Primary and Secondary Alkylboronates through Site-Selective C(sp3)–H Activation with Silica-Supported Monophosphine–Ir Catalysts
    Kawamorita, S.; Murakami, R; Iwai, T.; Sawamura, M.
    J. Am. Chem. Soc. 2013, 135, 2947–2950.
    DOI: 10.1021/ja3126239

 

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