Papers - Nakano Hiroto

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  1. アミノアルコールおよびその関連化合物を有機分子触媒として用いた不斉付加環化反応の開発

    中野博人,熊谷 淳,U. V. Subba Reddy,関 千草,奥山祐子,權 垠相,有機合成化学協会誌,vol.74,(7),(p.720 ~ 731 ),2016.08

  2. Catalytic efficiency of primary β-amino alcohols and their derivatives in organocatalysis

    Ummareddy Venkata Subba Reddy, Madhu Chennapuram, Chigusa Seki, Eunsang Kwon, Yuko Okuyama and Hiroto Nakano,European Journal of Organic Chemistry,(p.4124 ~ 4143),2016.06

  3. Simple Primary Amino Amide Organocatalyst for Enantioselective Aldol Reactions of Isatins with Ketones

    Jo Kimura, Ummareddy Venkata Subba Reddy, Yoshihito Kohari, Chigusa Seki, Yasuteru Mawatari, Koji Uwai, Yuko Okuyama, Eunsang Kwon, Michio Tokiwa, Mitsuhiro Takeshita, Tatsuo Iwasa and Hiroto Nakano,European Journal of Organic Chemistry,(p.3728 ~ 3756),2016.05

  4. 2-Azanorbornane-based amine organocatalyst for enantioselective aldol reaction of isatins with ketones

    Ayumi Ogasawara, U.V. Subba Reddy, Chigusa Seki, Yuko Okuyama, Koji Uwai, Michio Tokiwa, Mitsuhiro Takeshita, Hiroto Nakano,Tetrahedron: Asymmetry,vol.27,(20–21),(p.1062 ~ 1068),2016.05

  5. Chiral primary amino alcohol organobase catalysts for the asymmetric Diels-Alder reactions of anthrones with maleimides

    Jun Kumagai, Teppei Otsuki, U. V. Subba Reddy, Yoshihito Kohari, Chigusa Seki, Koji Uwai, Yuko Okuyama, Eunsang Kwon, Michio Tokiwa, Mitsuhiro Takeshita, Hiroto Nakano,Tetrahedron: Asymmetry,vol.26,(24),(p.1423 ~ 1439),2015.11

  6. Lipase-Catalyzed Domino Michael-Aldol Reaction of 2-Methyl-1,3-Cycloalkanedione and Methyl Vinyl Ketone for the Synthesis of Bicyclic Compounds

    Kaoru Sano, Yoshihito Kohari, Hiroto Nakano, Chigusa Seki, Mitsuhiro Takeshita, Michio Tokiwa, Yoshihiko Hirose, Koji Uwai,Synthetic Communications,vol.46,(1),(p.46 ~ 54),2015.11

  7. Silyloxy Amino Alcohol Organocatalyst for Enantioselective 1,3-Dipolar Cycloaddition of Nitrones to α,β- Unsaturated Aldehydes

    Teppei Otsuki, Jun Kumagai, Yoshihito Kohari, Yuko Okuyama, Eunsang Kwon, Chigusa Seki, Koji Uwai, Yasuteru Mawatari, Nagao Kobayashi, Tatsuo Iwasa, Michio Tokiwa, Mitsuhiro Takeshita, Atushi Maeda, Akihiko Hashimoto, Kana Turuga, Hiroto Nakano,European Journal of Organic Chemistry,vol.33,(33),(p.7292 ~ 7300),2015.10

  8. Chiral Primary Amino Amide Alcohol Organocatalyst for the Asymmetric Michael Addition of 4-Hydroxycoumarin with α,β-Unsaturated Ketones

    Jun Kumagai, Yoshihito Kohari, Chigusa Seki, Koji Uwai, Yuko Okuyama, Eunsang Kwon, Hiroto Nakano,Heterocycles,vol.20,(1),(p.1124 ~ 1134),2015.01

  9. Enantioselective Diels–Alder Reaction of 1,2-Dihydropyridines with Aldehydes Using β-Amino Alcohol Organocatalyst

    Yoshihito Kohari, Yuko Okuyama, Eunsang Kwon, Taniyuki Furuyama, Nagao Kobayashi, Teppei Otuki, Jun Kumagai, Chigusa Seki, Koji Uwai, Gang Dai, Tatsuo Iwasa, and Hiroto Nakano 79 (20), 9500-9511 (2014).,Journal of Organic Chemistry,vol.79,(20),(p.9500 ~ 9511),2014.11

  10. Chiral Oxazolidine Catalyst for Asymmetric Synthesis

    Hiroto Nakano, Yuko Okuyama, Eunsang Kwon,Heterocycles,vol.86,(1),(p.1 ~ 26),2014.01

  11. Development of a Novel Method for Warfarin Synthesis via Lipase-catalyzed Stereoselective Michael Reaction

    Kaoru Sano, Shun-ichi Saito, Yoshihiko Hirose, Yoshihito Kohari, Hiroto Nakano, Chigusa Seki, Michio Tokiwa, Mitsuhiro Takeshita, Koji Uwai,Heterocycles,vol.87,(2),(p.1269 ~ 1278),2013.05

  12. The develop of the catalytic asymmetric reaction using chiral oxazolidine

    中野博人, 奥山祐子, 竹下光弘, 權 垠相, 小針良仁, 松山春男,Synthetic Organic Chemistry,vol.70,(2),(p.142 ~ 153),2012.07

  13. Chiral primary amino silyl ether organocatalyst for the enantioselective Diels-alder reaction of 1,2-dihydropyridines with aldehydes

    Y. Sakuta, Y. Kohari, N. D. M. Romauli Hutabarat, K. Uwai, E. Kwon, Y. Okuyama, C. Seki, H. Matsuyama, N. Takano, M. Tokiwa, M. Takeshita, H. Nakano,Heterocycles,vol.86,(2),(p.1379 ~ 1388),2012.06

  14. new synthetic method of highly optical active tamifule intermediate using catalyst

    中野博人, 權 垠相, 奥山祐子,Fine Chemicals,vol.41,(6),(p.45 ~ 54),2012.06

  15. One step synthesis of optically active diazabicyclo[3.3.0]octanones or diazabicyclo[4.3.0]nonanones by asymmetric conjugate addition of cyclic hydrazine

    C. Seki, M. Hirama, T. Sato,S. Takeda, Y. Kohari, K. Ishigaki, M. Ohuchi, K. Yokoi, K. Uwai, N. Takano, H. Nakano, K. Umemura, H.Matsuyama,Heterocycles,vol.85,(1),(p.1045 ~ 1052),2012.02

  16. New hydrazine-based organocatalyst for asymmetric Diels-Alder reaction of 1,2-dihydropyridine

    Y. Okuyama, K. Osone, H. Nakano, M. Takeshita,Heterocycles,vol.84,(1),(p.1209 ~ 1216),2012.01

  17. Asymmetric synthesis of isoquinuclidine by Diels-Alder Reaction of 1,2-dihydropyridine and chiral dienophile utilizing a chiral Lewis acid

    M.Hirama, C. Suttibut, N. D. M. Romauli Hutabarat, C. Seki, N. Sakuta, T. Tsuchiya, Y. Kohari, H. Nakano, K. Uwai, N. Takano, M. Yasui, Y. Okuyama, K. Osone, M. Takeshita, H. Matsuyama,Heterocycles,vol.84,(1),(p.377 ~ 384),2012.01

  18. A highly enantioselective Diels-Alder reaction of 1,2-dihydropyridine using a simple β-aminoalcohol organocatalyst for a practical synthetic methodology of oseltamivir intermediate

    Chonticha Suttibut, Yoshihito Kohari, Ko Igarashi, Hiroto Nakano, Masafumi Hirama, Chigusa Seki, Haruo Matsuyama, Yuko Okuyama, Kenichi Osone, Mitsuhiro Takeshita, Eunsang Kwon,Tetrahedron Letters,vol.52,(9),(p.4745 ~ 4748),2011.08

  19. Efficient synthetic methodology of flav-3-enes using reductive elimination of flav-4-triflatebiflavones having a ring-a ring of two flavone units using Suzuki cross-coupling reactions

    Yoshihito Kohari, Yukio Hoshino, Haruo Matsuyama, Hiroto Nakano,Heterocycles,vol.82,(1),(p.843 ~ 850),2011.07

  20. New Hydrazine-type Organocatalyst in Asymmetric Diels-Alder Ewaction of 1,2-Dihydropyridines

    Yuko Okuyama,Kenichi Osone, Hiroto Nakano, Mitsuhiro Takeshita,Heterocycles,vol.84,(2),(p.1209 ~ 1216),2011.06

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