＜学歴・学位＞
東北大学　卒業
東北大学　大学院（薬学修士）
東北大学　大学院博士（薬学）

＜職歴＞
日清製粉株式会社　医薬研究所　研究員
東北薬科大学薬学部　講師
オハイオ州立大学　化学科　博士研究員
青森大学薬学部　非常勤講師
東北医科薬科大学薬学部　准教授

＜資格＞
薬剤師．危険物取扱者（甲種）

有機合成化学

・多機能性キラル合成素子の開発と医薬化学への応用
・不斉有機触媒を用いる多元的立体制御反応の開発

【researchmap】
https://researchmap.jp/read0055790

【著書】

• e-EROS Encyclopedia of Reagents for Organic Synthesis（John Wiley & Sons, Ltd.）, 2008

【論文】

• Ohno, S., Ito, M., Aoki, S., Inomata K.*, Regio- and stereoselective nucleophilic addition reactions of Swaminathan ketone and its methylated analog using organometallic reagents, Tetrahedron Lett., 132, 154800, 2023.
• Akahane, Y., Inomata K.*, Asymmetric intramolecular aldol reactions mediated by chiral triamines bearing a pyrrolidine scaffold to provide a Wieland–Miescher ketone, Heterocycles, 105, 566-575, 2022.
• Inomata K.*, Narita S , Novel stereoselective 1,2-rearrangement of Swaminathan ketone derivatives bearing a 7-membered ring under solvolysis conditions, Tetrahedron Lett., 61, 151542, 2020.
• Akahane Y., Miura A., Inomata, K.*, Alternative chiral preparations of a Swaminathan Ketone via asymmetric aldol reactions mediated by chiral amines bearing a pyrrolidine, Heterocycles, 100, 12-23, 2020.
• Honda S., Inomata K.*, Endo Y, Enantiodivergent synthesis of Wieland-Miescher ketone analog mediated by a chiral pyridinylmethylamine derivative, Heterocycles, 90, 950-966, 2015.
• Inomata K.*, Endo Y., Synthesis of 2-substituted 1,3-cycloheptanediones via a Lewis acid-mediated ring expansion reaction, Heterocycles, 88, 997-1012, 2014.
• Nagamine T., Inomata K.*, Endo Y., Paquette L. A.*, Amino Acid Mediated Intramolecular Asymmetric Aldol Reaction to Construct a New Chiral Bicyclic Enedione Containing a Seven-Membered Ring: Remarkable Inversion of Enantioselectivity Compared to the Six-Membered Ring Example, J. Org. Chem., 72, 123-131, 2007.
• Nagamine T., Inomata K.*, Endo Y., Paquette L. A.*, Amino Acid Mediated Intramolecular Asymmetric Aldol Reaction to Construct a New Chiral Bicyclic Enedione Containing a Seven-Membered Ring: Remarkable Inversion of Enantioselectivity Compared to the Six-Membered Ring Example, Chem. Pharm. Bull, 55, 1710-1712, 2007.
• Inomata K., Barrague M., Paquette L. A.*, Diastereoselectivities Realized in the Amino Acid Catalyzed Aldol Cyclizations of Triketo Acetonides of Differing Ring Size, J. Org. Chem., 70, 533-539, 2005.
• Suzuki K., Inomata K.*, Endo Y., Enantiocontrolled Synthesis of Jasmonates via Tandem Retro-Diels-Alder-Ene Reaction Activated by a Silyl Substituent, Org. Lett., 6, 409-411, 2004.
• Suzuki K., Inomata K.*, Enantiodivergent syntheses of gamma-substituted butenolides with tertiary and quaternary asymmetric centers, Tetrahedron Lett., 44, 745-749, 2003.
• Suzuki K., Inomata K.*, A new chiral route to optically pure (+)- and (-)-cis-endo-4-Oxatricyclo[5.2.1.02,6]dec-8-en-3-one, Synthesis, 1819-1822, 2002.

【特許】

• 上野正弘，川村恒二，猪股浩平，高橋敏博，6-(2-(R)-アミノプロピル)-1,4-ベンゾジオキサン-2-(R)-カルボン酸誘導体およびその製造方法, 特許番号4233135.
• 猪股浩平，高橋敏博，井上仁志，谷内誠，山崎博之，鈴木雅士，高沢努，川村恒二，押田紀男，池本裕之，岸江孝男，イソプレン誘導体,特許番号3888397.
• Takahashi T., Inomata, K., Oshida, N., Kubota, N., Hamada T., Iwata, M., 1,4－ベンゾジオキシン誘導体, WO1996/35685, 特許番号3068198.

【E－mail】inomata@iuhw.ac.jp