1	Stereoselective Construction of 1β-Azide- and 1β-Cyano-2-deoxyribose Derivatives Hiromichi Fujioka, Takahiro Moriya, Kazuhisa Okamoto, Yutaka Minamitsuji, Yoshifumi Ueyama, Nao Matsumoto, and Kenichi Murai Heterocycles in press (DOI: 10.3987/COM-14-S(K)86)
2	Selective Transformations of Carbonyl Functions in the Presence of α,​β-​Unsaturated Ketones: Concise Asymmetric Total Synthesis of Decytospolides A and B Yahata, Kenzo; Minami, Masaki; Watanabe, Kei; Fujioka, Hiromichi Organic Letters (2014), 16(14), 3680-3683.
3	C3-​Symmetric chiral trisimidazoline-​catalyzed Friedel-​Crafts (FC)​-​type reaction Takizawa, Shinobu; Hirata, Shuichi; Murai, Kenichi; Fujioka, Hiromichi; Sasai, Hiroaki Organic & Biomolecular Chemistry (2014), 12(31), 5827-5830.
4	Enantioselective iodolactonization of allenoic acids Murai, Kenichi; Shimizu, Nozomi; Fujioka, Hiromichi Chem. Commun. 2014, 50, 12530-12533.
5	Enantioselective, Desymmetrizing, Bromolactonization Reactions of Symmetric Olefinic Dicarboxylic Acids Kenichi Murai, Junki Nakajima, Akira Nakamura, Norimichi Hyogo, Hiromichi Fujioka Chem. Asian. J. (2014), 9, 3511-3517.
6	Selective Formation of Trans​/threo​/cis and Cis​/threo​/cis Bis-​tetrahydrofurans from the Same Diene Diols Fujioka, Hiromichi; Oki, Tomohiro; Hayashi, Tatsuya; Yamakawa, Maki; Kurachi, Takeshi; Nakahara, Kenji; Maehata, Ryota; Hamada, Tomohito; Murai, Kenichi; Kita, Yasuyuki Heterocycles (2014), 88(2), 1323-1336.
7	Rational hopping of a peptidic scaffold into non-peptidic scaffolds: structurally novel potent proteasome inhibitors derived from a natural product, belactosin A Shuhei Kawamura, Yuka Unno, Takatsugu Hirokawa, Akira Asai, Mitsuhiro Arisawa and Satoshi Shuto Chem. Commun.  (2014), 50, 2445-2447.
8	Structurally Novel Highly Potent Proteasome Inhibitors Created by the Structure-Based Hybridization of Non-Peptidic Belactosin Derivatives and Peptide Boronates Shuhei Kawamura, Yuka Unno, Akira Asai, Mitsuhiro Arisawa and Satoshi Shuto J. Med. Chem. (2014), 57, 2726-2735.
9	Palladium-Nanoparticle-Catalyzed Direct Ethynylation of Aliphatic Carboxylic Acid Derivatives via C(sp3)–H Bond Functionalization Mohammad Al-Amin, Mitsuhiro Arisawa, Satoshi Shuto, Yusuke Ano, Mamoru Tobisu and Naoto Chatani Adv. Synth. Catal. (2014), 356, 1631-1637.
10	Ligand-free Suzuki-Miyaura Coupling with Sulfur-modified Gold-supported Palladium in the Synthesis of a Conformationally-Restricted Cyclopropane Compound Library with Three-Dimensional Diversity Mitsuhiro Arisawa, Takatoshi Sato, Naoyuki Hoshiya, Mohammad Al-Amin, Yuji Kogami and Satoshi Shuto ACS Combi. Sci. (2014), 16, 215-220.
11	Palladium-Nanoparticle-Catalyzed 1,7-Palladium Migration Involving C-H Activation, Followed by Intramolecular Amination: Regioselective Synthesis of N1-Arylbenzotriazoles and an Evaluation of Their Inhibitory Activity Towards Indoleamine 2,3-Dioxygenase Koji Takagi, Mohammad Al-Amin, Naoyuki Hoshiya, Johan Wouters, Hiroshi Sugimoto, Yoshitsugu Shiro, Hayato Fukuda, Satoshi Shuto, Mitsuhiro Arisawa J. Org. Chem. (2014), 79, 6366-6371.
12	Development of a New Class of Proteasome Inhibitors with an Epoxyketone Warhead: Rational Hybridization of Non-peptidic Belactosin Derivatives and Peptide Epoxyketones Shuhei Kawamura, Yuka Unno, Akira Asai, Mitsuhiro Arisawa, Satoshi Shuto Bioorg. Med. Chem. (2014), 22, 3091-3095.
13	Conformationally Restricted GABA with Bicyclo[3.1.0]hexane Backbone as the First Highly Selective BGT-1 Inhibitor Takaaki Kobayashi, Akihiro Suemasa, Arisaw Igawa, Soichiro Ide, Hayato Fukuda, Hiroshi Abe, Mitsuhiro Arisawa, Masabumi Minami, Satoshi Shuto ACS Med. Chem. Lett. (2014),  in press

 

総説

1	In situ protection methodology in carbonyl chemistry Yahata, Kenzo; Fujioka, Hiromichi Chemical & Pharmaceutical Bulletin (2014), 62(1), 1-11.