UYANIK Muhammet (ウヤヌク ムハメット) プロフィール

名古屋大学

大学院工学研究科 化学・生物工学専攻 生物機能工学分野

バイオマテリアル講座 触媒有機合成学研究グループ 助教

 

所属学会
日本化学会

アメリカ化学会

有機合成化学協会

アメリカ科学振興協会

ヨウ素学会

 

muha[at]nubio.nagoya-u.ac.jp

TEL 052-789-3206 / FAX 052-789-3222


武波Gメンバー(2017年度)

西岡浩平(D2), 佐原直登(D1), 岩田寛和(M2), 片出旺太(M1), 田中啓貴(M1), 加藤丈裕(B4), 近藤竜太郎(B4)

卒業生

岡本寛晃(2011), 深津良太(2011), 金子恵里奈(2011), 中島大輔(2012), Dr.安井猛(2013), 大堀健人(2013), 永田大(2014), Dr.鈴木大介(2015), Dr.笹倉新葉(2015), 塚原万由子(2015), Dr.林裕樹(2016), 水野将宏(2016), 服部悠平(2016), 中嶋史雄(2016), Dr.六鹿達矢(2017),  請川直哉(2017), 小枝きらら(2017)

経歴

1981年 生まれ (トルコ国籍)

1998年 来日
2000年 国際学友会日本語学校卒業
2004年 名古屋大学工学部卒業
2006年 名古屋大学大学院工学研究科化学・生物工学専攻博士前期課程修了
2007年 名古屋大学大学院工学研究科化学・生物工学専攻博士後期課程修了 (石原一彰教授), 博士(工学)
学位論文: "ポリ環状テルペノイド類の全合成を指向したバイオミメティックポリエン環化反応の開発"

2004年〜2007年 文部科学省 国費外国人留学生
2007年 名古屋大学大学院工学研究科 助教 (石原一彰研究室)

賞歴

1998年 国際生物学オリンピックドイツ大会 銅メダル (トルコ代表)

2008年 第8回GSCシンポジウム ポスター賞
2008年 日本化学会第88春季年会 優秀講演賞 (学術)

2009年 2008年度有機合成化学協会研究企画賞 (塩野義製薬)
2009年 日本化学会第89春季年会 優秀講演賞 (学術)
2010年 平成22年度有機合成化学協会 東海支部奨励賞
2011年 第1回赤崎賞 (名古屋大学)

2012年 愛知県第6回わかしゃち奨励賞 最優秀賞
2012年 日本化学会第92春季年会 若い世代の特別講演会講演賞

2012年 第15回ヨウ素学会シンポジウム ポスター賞

2013年 科学技術分野の文部科学大臣 若手科学者賞

2015年 第7回井上リサーチアウォード

2015年 第4回GSC奨励賞

2015年 Banyu Chemist Award (BCA)

2016年 Thieme Chemistry Journal Award

2017年 日本化学会進歩賞

その他の活動

2013―2016 Turkish Journal of Chemistry 編集委員

2014―2016 有機合成化学協会誌 編集協力委員

Publication

40. Chiral Hypervalent Organoiodine-Catalyzed Enantioselective Oxidative Spirolactonization of Naphthol Derivatives

Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara

J. Org. Chem. 2017, 82, 11946–11953.

DOI: 10.1021/acs.joc.7b01941

39. alpha-Oxidation of Carbonyl Compounds

Muhammet Uyanik, Kazuaki Ishihara

In Science of Synthesis Reference Library: Catalytic Oxidation in Organic Synthesis, Kilian Muñiz (ed.), Georg Thieme-Verlag KG; 2017, pp. 635–670.

DOI; 10.1055/sos-SD-225-00320

38. 4,5-Dimethyl-2-Iodoxybenzenesulfonic Acid Catalyzed Site-Selective Oxidation of 2-Substituted Phenols to 1,2-Quinols

Muhammet Uyanik, Tatsuya Mutsuga, Kazuaki Ishihara

Angew. Chem. Int. Ed. 2017, 56, 3956–3960; Angew. Chem. 2017, 129, 4014–4018.

DOI: 10.1002/anie.201612463

37. Enantioselective Synthesis of Masked Benzoquinones Using Designer Chiral Hypervalent Organoiodine(III) Catalysis

Muhammet Uyanik, Niiha Sasakura, Masahiro Mizuno, Kazuaki Ishihara

ACS Catal. 2017, 7, 872–876.

DOI: 10.1021/acscatal.6b03380

36. Ammonium Hypoiodite-catalyzed Peroxidative Dearomatization of Phenols

Muhammet Uyanik, Kohei Nishioka, Kazuaki Ishihara

Heterocycles 2017, 95, 1132–1147.

DOI: 10.3987/COM-16-S(S)84

  • Special Issue in honor of Professor Dr. Masakatsu Shibasaki on 70th Birthday.

35. Chiral Quaternary Ammonium Hypoiodite Catalysis

Muhammet Uyanik, Kazuaki Ishihara

月刊ファインケミカル 2016, 45(12), 16–24.

特集号: ヨウ素触媒の開発最前線

34. Asymmetric Oxidative Dearomatization Reaction

Muhammet Uyanik, Kazuaki Ishihara

In Asymmetric Dearomatization Reactions, Shu-Li You (ed.), John Wiley & Sons; 2016, pp. 129–152.

DOI: 10.1002/9783527698479.ch6

33. Chiral Ammonium Hypoiodite Salt-Catalyzed Enantioselective Oxidative Cycloetherification to 2-Acyl Tetrahydrofurans

Muhammet Uyanik, Hiroki Hayashi, Hirokazu Iwata, Kazuaki Ishihara

Chem. Lett. 2016, 45, 353–355.

DOI: 10.1246/cl.160004

32. Practical Oxidative Dearomatization of Phenols with Sodium Hypochlorite Pentahydrate

Muhammet Uyanik, Niiha Sasakura, Mitsuyoshi Kuwahata, Yasukazu Ejima, Kazuaki Ishihara

Chem. Lett. 2015, 44, 381–383

DOI: 10.1246/cl.141130

31. High-Performance Hypoiodite/Hydrogen Peroxide Catalytic System for the Oxylactonization of Aliphatic γ-Oxocarboxylic Acids

Muhammet Uyanik, Daisuke Suzuki, Mizu Watanabe, Hiroyasu Tanaka, Kikuo Furukawa, Kazuaki Ishihara

Chem. Lett. 2015, 44, 387–389.

DOI: 10.1246/cl.141110

30. Chiral Ammonium Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of 1-Naphthols Using Hydrogen Peroxide

Muhammet Uyanik, Niiha Sasakura, Erina Kaneko, Kento Ohori, Kazuaki Ishihara

Chem. Lett. 2015, 44, 179–181.

DOI: 10.1246/cl.141012

  • Editor’s Choice

29. High-turnover hypoiodite catalysis for asymmetric synthesis of tocopherols

Muhammet Uyanik, Hiroki Hayashi, Kazuaki Ishihara

Science 2014, 345, 291–294.

DOI: 10.1126/science.1254976

28. Functional Group Transformations via Carbonyl Derivatives

Muhammet Uyanik, Kazuaki Ishihara

In Comprehensive Organic Synthesis, 2nd Edition, Gary A. Molander and Paul Knochel (eds.), Vol. 6, Oxford: Elsevier; 2014, pp. 573–597.

DOI: 10.1016/B978-0-08-097742-3.00622-4

27. 2-ヨードベンゼンスルホン酸(pre-IBS)とOxoneを用いる選択的酸化反応

Muhammet Uyanik, Tatsuya Mutsuga, Kazuaki Ishihara

和光純薬時報 2013, 81(4), 5–9.

26. Hydrogen Bonding and Alcohol Effects in Asymmetric Hypervalent Iodine Catalysis: Enantioselective Oxidative Dearomatization of Phenols

Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara

Angew. Chem. Int. Ed. 2013, 52, 9215–9218; Angew. Chem. 2013, 125, 9385–9388.

DOI: 10.1002/anie.201303559

  • Highlighted in Japanese Newspapers (Chunichi, Kagaku Kogyo Nippo).

25. Baeyer-Villiger Oxidation Using Hydrogen Peroxide

Muhammet Uyanik, Kazuaki Ishihara

ACS Catal. 2013, 3, 513–520. (Perspective)

DOI: 10.1021/cs300821u

24. Baeyer-Villiger Oxidation and Oxidative Cascade Reactions with Aqueous Hydrogen Peroxide Catalyzed by Lipophilic LiB(C6F5)4 or Ca[B(C6F5)4]2
Muhammet Uyanik, Daisuke Nakashima, Kazuaki Ishihara

Angew. Chem. Int. Ed. 2012, 51, 9093–9096; Angew. Chem. 2012, 124, 9227–9230.

DOI: 10.1002/anie.201204286

23. Conformationally-Flexible Chiral Hypervalent Organoiodine Catalysts for Enantioselective Oxidative Transformations
Muhammet Uyanik, Kazuaki Ishihara
J. Synth. Org, Chem., Jpn. 2012, 70, 1116–1122.

22. デザイン型ヨウ素触媒を用いる環境調和型選択的酸化反応

Muhammet Uyanik

化学と工業 2012, 65(8), 625–626.

21. 1,2-Benziodoxol-3(1H)-one, 1-Hydroxy, 1-Oxide (First Update)

Muhammet Uyanik, Kazuaki Ishihara

Electronic Encyclopedia of Reagents for Organic Synthesis (e-EROS), John Wiley & Sons. Published online, 14 September 2012.

DOI: 10.1002/047084289X.rn00236.pub2

20. IBS-Catalyzed Regioselective Oxidation of Phenols to 1,2-Quinones with Oxone
Muhammet Uyanik, Tatsuya Mutsuga, Kazuaki Ishihara

Molecules, 2012, 17, 8604–8616. (Special Issue: Hypervalent Compounds)

DOI: 10.3390/molecules17078604

19. 2-Iodoxy-5-Methylbenzenesulfonic Acid-Catalyzed Selective Oxidation of 4-Bromobenzyl Alcohol to 4-Bromobenzaldehyde or 4-Bromobenzoic Acid with Oxone
Muhammet Uyanik, Kazuaki Ishihara (checked by Richard Crockett, Margaret Faul)

Organic Syntheses, 2012, 89, 105–114.

DOI: 10.15227/orgsyn.089.0105

18. Catalysis with In Situ-Generated (Hypo)iodite Ions for Oxidative Coupling Reactions

Muhammet Uyanik, Kazuaki Ishihara

ChemCatChem 2012, 4, 177–185. (Concept Article)

DOI: 10.1002/cctc.201100352

  • Selected as Very Important Paper (VIP).

17. In Situ Generated (Hypo)Iodite Catalysts for the Direct alpha-Oxyacylation of Carbonyl Compounds with Carboxylic Acids
Muhammet Uyanik, Daisuke Suzuki, Takeshi Yasui, Kazuaki Ishihara

Angew. Chem. Int. Ed. 2011, 50, 5331–5334; Angew. Chem. 2011, 123, 5443–5446.

DOI: 10.1002/anie.201101522

  • Highlighted in Japanese Newspaper (Nikkan Kogyo Shinbun).
  • Highlighted in Pharmacia (by Miyamoto Kazunori, 2012, 48(3), 237).
  • Highlighted in TCI Topics.

16. In Situ-Generated Chiral Quaternary Ammonium (Hypo)iodite Catalysis for Enantioselective Oxidative Cyclisations
Muhammet Uyanik, Kazuaki Ishihara

Chimica Oggi-Chemistry Today, 2011, 29, 18–21.

15. 非共有結合相互作用を利用したキラル超原子価ヨウ素触媒の開発:北スピロラクトン化反応への応用

Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara

和光純薬時報 2011, 79(2), 2–5.

14. Chiral Hypervalent Iodine-Catalyzed Enantioselective Oxidative Kita Spirolactonization of 1-Naphthol Derivatives and One-Pot Diastereoselective Oxidation to Epoxyspirolactones
Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara
Tetrahedron 2010, 66, 5841–5851.

DOI: 10.1016/j.tet.2010.04.060

  • Special Issue: Hypervalent Iodine Chemistry.
  • Highlighted in Synfacts 2010, 9, 1000.
  • Recognized by Elsevier as one of their "Top-25 most cited articles" as published in Tetrahedron for 2010-2011.

13. 金属を使わない不斉酸化的カップリング触媒、無機ヨウ素酸塩へのブレークスルー

Kazuaki Ishihara, Muhammet Uyanik

化学 2010, 65(10), 12–17.

12. Quaternary Ammonium (Hypo)iodite Catalysis for Enantioselective Oxidative Cycloetherification
Muhammet Uyanik, Hiroaki Okamoto, Takeshi Yasui, Kazuaki Ishihara
Science 2010, 328, 1376–1379.

DOI: 10.1126/science.1188217

11. Enantioselective Kita Oxidative Spirolactonization Catalyzed by In Situ Generated Chiral Hypervalent Iodine(III) Species
Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara
Angew. Chem. Int. Ed. 2010, 49, 2175–2177; Angew. Chem. 2010, 122, 2221–2223.

DOI: 10.1002/anie.200907352

  • Selected as “Hot Paper” and “Front Cover” (Issue 12).
  • Press Release from Nagoya University.
  • Highlighted in Japanese Newspapers (Chunichi, Yomiuri, Mainichi, Nikkan Kogyo, Kagaku Kogyo Nippo, Jiji Press, Kyodo Press, Yahoo News, etc.).
  • Rank in Most Accessed Articles (Mar 2010).
  • Highlighted in Synfacts 2010, 5, 602.
  • Highlighted in Journal of Synthetic Organic Chemistry, Japan 2011, 69(1), p86.
  • Chiral iodoarene pre-catalyst [(2R,2R’)-2,2’-(2-iodo-1,3-phenylene)bis(oxy)bis(N-mesitylpropanamine)] is commercially available from Wako Pure Chemical Industries, Ltd. and TCI Co., Ltd.

10. 2-Iodoxybenzenesulfonic Acid (IBS)-Catalyzed Oxidation of Alcohols

Muhammet Uyanik, Kazuaki Ishihara

Aldrichim. Acta 2010, 43(3), 83–91.

9. 2-Iodobenzenesulfonic Acid

Muhammet Uyanik, Kazuaki Ishihara

Electronic Encyclopedia of Reagents for Organic Synthesis (e-EROS), John Wiley & Sons. Published online, 15 October 2010.

DOI: 10.1002/047084289X.rn01214.pub2

8. Bromine Catalyzed Aerobic Oxidation of Alcohols
Muhammet Uyanik, Ryota Fukatsu, Kazuaki Ishihara
Chem. Asian J. 2010, 5, 456–460.

DOI: 10.1002/asia.200900609

  • Rank in Most Accessed Articles for monthly (Feb. 2010) and for the year (2009-2010).
  • Highlighted in Journal of Synthetic Organic Chemistry, Japan 2010, 68(8), p873.

7. Hypervalent Iodine-Catalyzed Oxylactonization of Ketocarboxylic Acids to Ketolactones
Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara
Bioorg. Med. Chem. Lett. 2009, 19, 3848–3851.

DOI: 10.1016/j.bmcl.2009.03.148

  • Special Issue: the 2009 Tetrahedron Young Investigator Award in Bioorgaic and Medicinal Chemistry in honor of its recipient Prof. C. F. Barbas.

6. IBS-Catalyzed Oxidative Rearrangement of Tertiary Allylic Alcohols to Enones with Oxone
Muhammet Uyanik, Ryota Fukatsu, Kazuaki Ishihara
Org. Lett. 2009, 11, 3470–3473.

5. Hypervalent Iodine Mediated Oxidation of Alcohols

Muhammet Uyanik, Kazuaki Ishihara

Chem. Commun. 2009, 45, 2086–2099. (Feature Article)

DOI: 10.1039/B823399C

  • Rank in ChemComm Most Cited Feature Articles 2009 Top 10.

4. 2-Iodoxybenzenesulfonic Acid as an Extremely Active Catalyst for the Selective Oxidation of Alcohols to Aldehydes, Ketones, Carboxylic Acids, and Enones with Oxone
Muhammet Uyanik, Matsujiro Akakura, Kazuaki Ishihara
J. Am. Chem. Soc. 2009, 131, 251–262.

3. Catalytic Diastereoselective Polycyclization of Homo(polyprenyl)arene Analogues Bearing Terminal Siloxyvinyl Groups
Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto
Org. Lett. 2006, 8, 5649–5652.

2. Biomimetic Synthesis of Acid-Sensitive (-)- and (+)-Caparrapi Oxides, (-)- and (+)-8-Epicaparrapi Oxides, and (+)-Dysifragin Induced by Artificial Cyclases
Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto
Bioorg. Med. Chem. 2005, 13, 5055–5065.

DOI: 10.1016/j.bmc.2005.04.029

  • Special Issue: Chemistry and Biology of Natural Products-Tetrahedron Prize for Creativity in Organic Chemistry 2004: K. Nakanishi.

1. Biomimetic Synthesis of Acid-Sensitive (-)-Caparrapi Oxide and (+)-8-Epicaparrapi Oxide Induced by Artificial Cyclases
Muhammet Uyanik, Hideaki Ishibashi, Kazuaki Ishihara, Hisashi Yamamoto
Org. Lett. 2005, 7, 1601–1604.

特許

1. カルボニル化合物の製造方法 (Method for producing carbonyl compound)

Kazuaki Ishihara, Muhammet Uyanik (National University Corporation, Nagoya University)

JP Patent Pub. No. JP2008-247872(A), 2008.10.16 (Appl. No. JP2007-94377, 2007.3.30).

 

2. カルボニル化合物の製造方法およびカルボニル化合物の製造に用いる酸化促進剤 (Method for producing carbonyl compound and pro-oxidant used for production of carbonyl compound)

Kazuaki Ishihara, Muhammet Uyanik, Yukihiro Isogai, Suguru Ohara (National University Corporation, Nagoya University)

JP Patent Reg. No. JP4590514(B2), 2010.9.24 (Pub. No. JP2010-100636(A), 2010.5.6; Appl. No. JP2009-284483, 2009.12.15; Priority No. JP2007-0226843, 2007.8.31).

PCT Pub. No. WO2009-028676(A1), 2009.3.5 (Appl. No. WO2008-JP65567, 2008.8.29).

EP Patent Reg. No. EP2085373(B1), 2013.1.16 (Pub. No. EP2085373(A1), 2009.8.5; Appl. No. EP2008-828094, 2008.8.29).

US Patent Reg. No. US8394995(B2), 2013.3.12 (Pub. No. US2010-0041917(A1), 2010.2.18; Appl. No. US2009-441194, 2008.8.29).

CN Patent Reg. No. CN101541725(B), 2013.8.28 (Pub. No. CN101541725(B), 2009.9.23; Appl. No. CN2008-80000718, 2008.8.29).

 

3. 光学活性な環状エーテル化合物の製法及びそれに用いる触媒 (Method for producing optically active cyclic ether compound and catalyst used for the same)

Kazuaki Ishihara, Muhammet Uyanik (National University Corporation, Nagoya University)

JP Patent Reg. No. JP5544596(B2), 2014.5.23 (Pub. No. JP2011-57648, 2011.3.24; Appl. No. JP2009-211609, 2009.9.14).

 

4. ヨードベンゼン誘導体及びそれを用いた光学活性スピロラクトン化合物の製法 (Iodobenzene derivative and process for preparation of optically active spirolactone compound using same)

Kazuaki Ishihara, Muhammet Uyanik (National University Corporation, Nagoya University)

JP Patent Reg. No. JP5747332(B2), 2015.5.22 (Pub. No. JP WO2011-052388(A1), 2011.5.5; Appl. No. JP2011-538342, 2010.10.14; Priority No. JP2009-245275, 2009.10.26).

PCT Pub. No. WO2011-052388(A1), 2011.5.5 (Appl. No. WO2010-JP068031, 2010.10.14).

 

5. α-アシロキシカルボニル化合物の製法及び新規なα-アシロキシルカルボニル化合物 (Method for producing α-acyloxycarbonyl compound and novel α-acyloxycarbonyl compound)

Kazuaki Ishihara, Muhammet Uyanik (National University Corporation, Nagoya University; Mitsubishi Rayon Co., Ltd.)

JP Patent Reg. No. JP5770160(B2), 2015.7.3 (Pub. No. JP WO2011-108696 (A1), 2011.9.9; Appl. No. JP2012-503280, 2011.3.4; Priority No. JP2010-049003, 2010.3.5).

PCT Pub. No. WO2011-108696(A1), 2011.9.9 (Appl. No. WO2011-JP55043, 2011.3.4).

EP Patent Reg. No. EP2543658(B1), 2015.5.6 (Pub. No. EP2543658(A1), 2013.1.9; Appl. No. EP2011-0750805, 2011.3.4).

US Patent Reg. No. US8680322(B2), 2014.3.25 (Pub. No. US2012-0323014(A1), 2012.12.20; Appl. No. US2011-13581734, 2011.3.4).

CN Patent Reg. No. CN102834368(B), 2015.4.1 (Pub. No. CN102834368(A), 2012.12.19; Appl. No. CN2011-812595, 2011.3.4).

CN Patent Reg. No. CN103864608(B), 2016.3.16 (Appl. No. CN2014-178904, 2011.3.4).

TW Patent Reg. No. TWI516473(B), 2016.1.11 (Pub. No. TW201139360(A), 2011.11.16; Appl. No. TW2011-0107298, 2011.3.4).

KR Patent Pub. No. KR20130004282(A), 2013.1.9 (Appl. No. KR2012-7023122, 2011.3.4).

 

6. エステルの製法 (Method for producing esters)

Kazuaki Ishihara, Muhammet Uyanik (National University Corporation, Nagoya University)

JP Patent Reg. No. JP5920889(B2), 2016.4.22 (Pub. No. JP WO2012-060185(A1), 2012.5.10; Appl. No. JP2012-541793, 2011.10.11; Priority No. JP2010-245944, 2010.11.2).

PCT Pub. No. WO2012-060185(A1), 2012.5.10 (Appl. No. WO2011-JP73340, 2011.10.11).

EP Patent Reg. No. EP2636665(B1), 2016.6.22 (Pub. No. EP2636665(A1), 2013.9.11; Appl. No. EP2011-0837836, 2011.10.11).

US Patent Reg. No. US8853426(B2), 2014.10.7 (Pub. No. US2013-0217898(A1), 2013.8.22; Appl. No. US2011-13881544, 2011.10.11).

 

7. 窒素原子又は酸素原子を含む環構造を有する芳香族化合物の製造方法 (Method for producing aromatic compound having ring structure that includes nitrogen atom or oxygen atom)

Kazuaki Ishihara, Muhammet Uyanik (National University Corporation, Nagoya University)

JP Patent Reg. No. JP5929767(B2), 2016.5.13 (Pub. No. JP WO2012-111449(A1), 2012.8.23; Appl. No. JP2012-557880, 2012.2.2; Priority No. JP2011-033808, 2011.2.18).

PCT Pub. No. WO2012-111449(A1), 2012.8.23 (Appl. No. WO2012-JP52424, 2012.2.2).

US Patent Reg. No. US9018394(B2), 2015.4.28 (Pub. No. US2013-0338371(A1), 2013.12.19; Appl. No. US2012-13982424, 2012.2.2).

 

8. ヨードアレーン誘導体、それを用いた光学活性スピロラクトン化合物の製法及び光学活性な環化付加体の製法 (Iodoarene derivative, method for producing optically active spirolactone compound using same, and method for producing optically active cyclization adduct)

Kazuaki Ishihara, Muhammet Uyanik, Takeshi Yasui (National University Corporation, Nagoya University)

JP Patent Reg. No. JP5688647(B2), 2015.2.6 (Pub. No. JP WO2012-121248(A1), 2012.9.13; Appl. No. JP2013-503554, 2012.3.6; Priority No. JP2011-052572, 2011.3.10).

PCT Pub. No. WO2012-121248(A1), 2012.9.13 (Appl. No. WO2012-JP055679, 2012.3.6).

EP Patent Pub. No. EP2684863(A1), 2014.1.15 (Appl. No. EP2012-0754890, 2012.3.6).

US Patent Reg. No. US9000216(B2), 2015.4.7 (Pub. No. US2013-0338364(A1), 2013.12.19; Appl. No. US2012-14002574, 2012.3.6).

CN Patent Pub. No. CN103415501(A), 2013.11.27 (Appl. No. CN2012-812292, 2012.3.6).

 

9. ビアリール化合物の製造方法 (Production method for biaryl compound)

Kazuaki Ishihara, Muhammet Uyanik (National University Corporation, Nagoya University)

JP Patent Appl. No. JP2012-031223, 2012.2.16.

PCT Pub. No. WO2013-121873(A1), 2013.8.22 (Appl. No. WO2012-JP51838, 2013.1.29).

 

10. 含窒素環化合物の製造方法 (Production method for nitrogen-containing cyclic compound, and nitrogen-containing cyclic compound)

Kazuaki Ishihara, Muhammet Uyanik (National University Corporation, Nagoya University)

JP Patent Appl. No. JP2012-031224, 2012.2.16.

PCT Pub. No. WO2013-121879(A1), 2013.8.22 (Appl. No. WO2012-JP51983, 2013.1.30).

 

11. 光学活性2-アシルクロマン化合物の製法およびそれに用いる触媒前駆体 (Method for producing optically active 2-acylchroman compound and precatalyst used for the same)

Kazuaki Ishihara, Muhammet Uyanik (National University Corporation, Nagoya University)

JP Patent Reg. No. JP6004330(B2), 2016.9.16 (Pub. No. JP2014-51437(A), 2014.3.20; Appl. No. JP2012-194893, 2012.9.5).

 

12. 窒素原子を含む環構造を有する光学活性な芳香族化合物の製法 (Method for producing optically active aromatic compounds having ring structure that includes nitrogen atom)

Kazuaki Ishihara, Muhammet Uyanik, Daisuke Suzuki (National University Corporation, Nagoya University)

JP Patent Reg. No. JP6115946(B2), 2017.3.31 (Pub. No. JP2014-240365(A), 2014.12.25; Appl. No. JP2013-123423, 2013.6.12).

 

13. アリールヒドロキノン類の製法及びアリールキノン類の製法 (Method for producing aryl hydroquinone derivative and aryl quinone derivative)

Kazuaki Ishihara, Muhammet Uyanik (National University Corporation, Nagoya University)

JP Patent Pub. No. JP2015-168660, 2015.9.28 (Appl. No. JP2014-046259, 2014.3.10).

 

14. 新規なアルキルカルボニルラクトン化合物及びその製造方法 (New alkyl carbonyl lactone compounds and method for producing thereof)

Kazuaki Ishihara, Muhammet Uyanik, Kikuo Furukawa, Hiroyasu Tanaka (National University Corporation, Nagoya University; Mitsubishi Gas Co. Ltd.)

JP Patent Pub. No. JP2016-74614, 2016.5.12 (Appl. No. JP2014-204756, 2014.10.3).

外部獲得資金

2007    JST 研究成果展開支援プログラム「シーズ発掘試験」(08-477)

2010-2012 科学研究費補助金 若手研究_B (20245022)

2010    JST 研究成果最適展開支援事業(A-STEP)-探索タイプ (AS221Z02039D)

2011-2012 JST 研究成果最適展開支援事業(A-STEP)-探索タイプ (AS232Z02306D)

2012-2013 JST 研究成果最適展開支援事業(A-STEP)-探索タイプ (AS242Z00126M)

2012-2013 JST 復興促進プログラム(A-STEP)-探索タイプ (241FT0209)

2013    科学研究費補助金 挑戦的萌芽研究 (25620078)

2013-2014 科研費・新学術領域研究「分子活性化」公募研究 (25105722)

2015-2017 科学研究費補助金 若手研究_A (15H05484)

試薬化

Sodium 2-iodobenzenesulfonate (Pre-IBS) (CAS: 62973-39-7)

Junsei Chemical Ltd.: 80517-1615 (1g).

Potassium 2-iodobenzenesulfonate (Pre-IBS) (CAS: 62973-69-7)

Junsei Chemical Ltd.: 80516-1615 (1g).

Potassium 2-iodo-5-methylbenzenesulfonate (Pre-MIBS)(CAS: 1093215-92-9)

Sigma-Aldrich: 720011-(1g, 5g, 10g)

Junsei Chemical Ltd.: 80545-1615 (1g).

Wako Pure Chemical Industries, Ltd.: 167-25741 (100mg)163-25743 (1g), 161-25744 (5g).

(R,R)-2-Iodo-1,3-bis[1-(mesitylcarbamoyl)ethoxy]benzene (CAS: 1226896-38-3)

Wako Pure Chemical Industries, Ltd.: 095-06051 (250 mg), 091-06053 (1 g).

TCI Co. Ltd.: I0807 (200 mg).

Recruit

ポスドク及び大学院生を募集中です。

当研究室では学部生、大学院生の研究室見学を随時受け付けております。

希望者は、石原教授までメールでお問い合わせ下さい。

 

Postdoctoral and graduate students is being recruited.In our laboratory will be accepted at any time undergraduate, graduate student visits to laboratories.Those who wish, please contact us by e-mail to Professor Ishihara.

Access

ISHIHARA GROUP

名古屋大学

大学院工学研究科 有機・高分子化学専攻(工学部 化学生命工学科)
有機化学講座

触媒有機合成学研究グループ

〒464-8603 名古屋市千種区不老町

B2-3(611)

 

Laboratory of Catalysis in Organic Synthesis, Research Group of Molecular Chemistry, Graduate Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering (Undergraduate Department of Chemistry and Biotechnology, School of Engineering), Nagoya University

B2-3(611), Furo-cho, Chikusa, Nagoya 464-8603, Japan