Publications

181 papers　Bold: lab members

2026(2)

Mitsuda, Y.; Kotani, S.; Wada, M. Suppressive Effect of Chrysanthemum × morifolium Ramat. on Type I Hypersensitivity Reactions and Its Molecular Mechanism J. Med. Food 2026, 29, 137–146. DOI
Kagami, A.; Hashimoto, N.; Sasaki, R.; Fukushima, Y.; Devkota, H. P.; Tanaka, S.; Wada, M.; Yamanaka, K.; Yamakawa, S.; Misumi, S.; Yokoyama, T.; Mizuguchi, M.; Sato, T.; Nakamura, T.; Kotani, S.; Suico, M. A.; Kai, H.; Ueda, M.; Shuto, T. Glycosidic scaffold bearing multiple galloyl moieties from pomegranate disrupts transthyretin amyloids iScience 2026, 29, 114170. DOI

2025(5)

Hori, K.; Kurauchi, Y.; Kotani, S.; Devkota, H. P. Analysis of Functional Compounds in Matcha by Quantitative Nuclear Magnetic Resonance Spectroscopy Sci. Pharm. 2025, 93, 11. DOI
Sadahiro, Y.; Okubo, M.; Hitora, Y.; Hitora-Imamura, N.; Kotani, S.; Tsukamoto, S. Pestones A and B from a Fungus Pestalotiopsis sp. Bound to Mutant p53 and Changed Its Conformation J. Nat. Prod. 2025, 88, 546–553. DOI
Sadahiro, Y.; Okubo, M.; Hitora, Y.; Hitora-Imamura, N.; Kotani, S.; Tsukamoto, S. Correction to Pestones A and B from a Fungus Pestalotiopsis sp. Bound to Mutant p53 and Changed its Conformation J. Nat. Prod. 2025, 88, 1868. DOI
Imai, T.; Isasaka, M.; Oyama, Y.; Takagi, Y.; Ohura, K.; Kotani, S.; Nakadae, Y. Functional analysis of modified caco-2 cells carrying CES2A1 as a model for intestinal absorption of prodrugs Biol. Pharm. Bull. 2025, 48, 162–171. DOI
Arae, S.; Shimoda, Y.; Kuwajima, M.; Kotani, S.; Nakajima, M. Three- and Seven-membered Annulenones as a Lewis Base Catalyst for Enantioselective meso-Epoxide Opening Adv. Synth. Catal. 2025, 367, e202401186. DOI

2024(3)

Kotani, S.; Asano, T.; Arae, S.; Sugiura, M.; Nakajima, M. Mechanistic Investigations of Chiral Lithium Binaphtholate Catalysis for Asymmetric Aldol–Tishchenko Reaction of α-Fluoroarylketones J. Org. Chem. 2024, 89, 17101–17114. DOI
Nakanishi, R.; Kurauchi, Y.; Kotani, S.; Hitora-Imamura, N.; Seki, T.; Katsuki, H. Structurally distinct Nurr1 ligands exhibit different pharmacological characteristics in regulating inflammatory responses of microglial BV-2 cells Biol. Pharm. Bull. 2024, 47, 1937–1945. DOI
Kinoshita, K.; Motomura, K.; Ushida, K.; Hirata, Y.; Konno, A.; Hirai, H.; Kotani, S.; Hitora-Imamura, N.; Kurauchi, Y.; Seki, T.; Katsuki, H. Nurr1 overexpression in the primary motor cortex alleviates motor dysfunction induced by intracerebral hemorrhage in the striatum in mice Neurotherapeutics 2024, 21, e00370. DOI

2023(5)

El-Desoky, A. H.; Asano, T.; Maeyama, Y.; Kato, H.; Hitora, Y.; Goto, E.; Kotani, S.; Nakajima, M.; Tsukamoto, S. Arteperoxides A-C, tris-normonoterpene-sesquiterpene conjugates with peroxide-bridges from Artemisia judaica exhibiting antiosteoclastogenic activity Phytochemistry 2023, 206, 113548. DOI
Sasaki, R.; Suico, M. A.; Chosa, K.; Teranishi, Y.; Sato, T.; Kagami, A.; Kotani, S.; Kato, H.; Hitora, Y.; Tsukamoto, S.; Yamashita, T.; Yokoyama, T.; Mizuguchi, M.; Kai, H.; Shuto, T. Combinatorial screening for therapeutics in ATTRv amyloidosis identifies naphthoquinone analogues as TTR-selective amyloid disruptors J. Pharmacol. Sci. 2023, 151, 54–62. DOI
Kuwazuru, J.; Suico, M. A.; Omachi, K.; Kojima, H.; Kamura, M.; Kaseda, S.; Kawahara, T.; Hitora, Y.; Kato, H.; Tsukamoto, S.; Wada, M.; Asano, T.; Kotani, S.; Nakajima, M.; Misumi, S.; Sannomiya, Y.; Horizono, J.; Koyama, Y.; Owaki, A.; Shuto, T.; Kai, H. CyclosporinA Derivative as Therapeutic Candidate for Alport Syndrome by Inducing Mutant Type IV Collagen Secretion Kidney360 2023, 4, 909–917. DOI
Harada, N.; Asano, T.; Sugiura, M.; Kotani, S.; Nakajima, M. Lithium binaphtholate-catalyzed asymmetric Michael reaction of acrylamides Chem. Pharm. Bull. 2023, 71, 792–797. DOI
Yoshiwara, Y.; Kotani, S.; Nakajima, M. Enantioselective and Chemoselective Phosphine Oxide-catalyzed Aldol Reaction of N-Unprotected Cyclic Carboxyimides Chem. Eur. J. 2023, e202203506. DOI

2022(3)

Nakajima, M.; Kotani, S.; Sugiura, M. Enantioselective Epoxide Opening Org. React. 2022, 110, 655–902. DOI
El-desoky, A. H. H.; Eguchi, K.; Kishimoto, N.; Asano, T.; Kato, H.; Hitora, Y.; Kotani, S.; Nakamura, T.; Tsuchiya, S.; Kawahara, T.; Watanabe, M.; Wada, M.; Nakajima, M.; Watanabe, T.; Misumi, S.; Tsukamoto, S. Isolation, Synthesis, and Structure-Activity Relationship Study on Daphnane and Tigliane Diterpenes as HIV Latency-Reversing Agents J. Med. Chem. 2022, 65, 3460–3472. DOI
Kinoshita, K.; Yoshimizu, A.; Ichihara, Y.; Ushida, K.; Kotani, S.; Kurauchi, Y.; Seki, T.; Katsuki, H. A Nurr1 ligand C-DIM12 attenuates brain inflammation and improves functional recovery after intracerebral hemorrhage in mice Sci. Rep. 2022, 12, 11009. DOI

2021(5)

Kobashigawa, Y.; Ohara, T.; Morita, K.; Toyota, Y.; Nakamura, T.; Kotani, S.; Arimori, T.; Yamauchi, S.; Liu, C.; Kitazaki, M.; Wakeyama-Miyazaki, Y.; Suwa, Y.; Uchida-Kamekura, M.; Fukuda, N.; Sato, T.; Nakajima, M.; Takagi, J.; Yamagata, Y.; Morioka, H. Molecular recognition of a single-chain Fv antibody specific for GA-pyridine, an advanced glycation end-product (AGE), elucidated using biophysical techniques and synthetic antigen analogs J. Biochem. 2021, 170, 379–387. DOI
Kotani, S.; Tashima, Y.; Tanaka, H.; Aoki, S.; Nakajima, M. Chiral Phosphine Oxide-Catalyzed Enantioselective Ring Opening of Oxetanes Heterocycles 2021, 103, 1048–1056. DOI
Sugiura, M.; Kotani, S.; Nakajima, M. Catalysis by Silicon Species Catalysis with Earth-Abundant Elements (RSC Catalysis Series) 2021, 40, 309–333.
Kai, H.; Shuto, T.; Suico, M. A.; Tsukamoto, S.; Misumi, S.; Kawahara, T.; Hitora, Y.; Kato, H.; Kotani, S.; Araki, K. Drug for curative therapy of intractable hereditary renal Alport syndrome containing cyclophilin D inhibitor WO2021049633 (2021).
Hori, Y.; Tsutsumi, R.; Nasu, K.; Boateng, A.; Ashikari, Y.; Sugiura, M.; Nakajima, M.; Kurauchi, Y.; Hisatsune, A.; Katsuki, H.; Seki, T. Aromatic-Turmerone Analogs Protect Dopaminergic Neurons in Midbrain Slice Cultures through Their Neuroprotective Activities Cells 2021, 10, 1090. DOI

2020(7)

Itoi, H.; Kotani, S.; Tanabe, Y.; Kasai, Y.; Suzuki, R.; Miyaji, M.; Iwata, H.; Ohzawa, Y. Study of the mesopore size effect on the electrochemical capacitor behaviors of mesoporous carbon/quinone derivative hybrids Electrochim. Acta 2020, 362, 137119. DOI
Kotani, S.; Nakajima, M. Asymmetric cross-aldol reactions between two carbonyl compounds catalyzed by chiral phosphine oxides J. Synth. Org. Chem., Jpn. 2020, 78, 1163–1173.
Boateng, A.; Harada, T.; Ashikari, Y.; Nakajima, M.; Sugiura, M. Synthesis of conjugated multiunsaturated thioesters via one-pot TiCl4-promoted aldol condensation Tetrahedron Lett. 2020, 61, 152280. DOI
Kotani, S.; Nakajima, M. Recent Advances in Asymmetric Phosphine Oxide Catalysis Tetrahedron Lett. 2020, 61, 151421. DOI
Yoshimitsu, T.; Kuboyama, Y.; Nishiguchi, S.; Nakajima, M.; Sugiura, M. O-Monoacyltartaric Acid/(Thio)urea Cooperative Organocatalysis for Enantioselective Conjugate Addition of Boronic Acid Org. Lett. 2020, 22, 3780–3784. DOI
Kotani, S.; Hanamure, T.; Mori, Y.; Nakajima, M. Phosphine-oxide-catalyzed Enantioselective Cross-aldol Reaction of Aldehydes with Trichlorosilane as Lewis Acid Promoter ChemCatChem 2020, 12, 4780–4783. DOI
Oniki, K.; Kawakami, T.; Nakashima, A.; Miyata, K.; Watanabe, T.; Fujikawa, H.; Nakashima, R.; Nasu, A.; Eto, Y.; Takahashi, N.; Nohara, H.; Suico, M. A.; Kotani, S.; Obata, Y.; Sakamoto, Y.; Seguchi, Y.; Saruwatari, J.; Imafuku, T.; Watanabe, H.; Maruyama, T.; Kai, H.; Shuto, T. Melinjo seed extract increases adiponectin multimerization in physiological and pathological conditions Sci. Rep. 2020, 10, 4313. DOI

2019(5)

Sugiura, M.; Ashikari, Y.; Takahashi, Y.; Yamaguchi, K.; Kotani, S.; Nakajima, M. Lewis Base-catalyzed Enantioselective Conjugate Reductions of β,β-Disubstituted α,β-Unsaturated Ketones with Trichlorosilane J. Org. Chem. 2019, 84, 11458–11473. DOI
Hashimoto, Y.; Michimuko, C.; Yamaguchi, K.; Nakajima, M.; Sugiura, M. Selective Monoacylation of Diols J. Org. Chem. 2019, 84, 9313–9321. DOI
Kotani, S. Phosphine oxide-catalyzed asymmetric aldol reactions and double aldol reactions Chem. Pharm. Bull. 2019, 67, 519–526. DOI
Sakamoto, M.; Kaneko, T.; Orito, Y.; Shimoda, Y.; Nakajima, M. Lithium Binaphtholate-Catalyzed Michael Reaction of Malonates Chem. Pharm. Bull. 2019, 67, 452–446. DOI
Asano, T.; Kotani, S.; Nakajima, M. Stereoselective Synthesis of 2-Fluoro-1,3-diols via Lithium Binaphtholate-catalyzed Aldol–Tishchenko Reaction Org. Lett. 2019, 21, 4192–4196. DOI

2018(2)

Kotani, S.; Yoshiwara, Y.; Ogasawara, M.; Sugiura, M.; Nakajima, M. Catalytic Enantioselective Aldol Reactions of Unprotected Carboxylic Acids under Phosphine Oxide Catalysis Angew. Chem. Int. Ed. 2018, 57, 15877–15881. DOI
Nakajima, M.; Watanabe, R.; Osakama, K.; Sakamoto, M.; Takemoto, D.; Kukita, K. Dramatic Enantioselectivity Reversal Heterocycles 2018, 97, 708–711. DOI

2017(7)

Asano, T.; Moritani, M.; Nakajima, M.; Kotani, S. Chiral lithium binaphtholate for enantioselective amination of acyclic α-alkyl-β-keto esters: Application to the total synthesis of L-carbidopa Tetrahedron 2017, 73, 5975–5982. DOI
Kotani, S.; Hanamure, T.; Nozaki, H.; Sugiura, M.; Nakajima, M. Enantioselective chlorinative aldol reaction of α-substituted acroleins catalyzed by chiral phosphine oxides Tetrahedron: Asymmetry 2017, 28, 282–287. DOI
Sugiura, M.; Kashiwagi, T.; Ito, M.; Kotani, S.; Nakajima, M. Stereoselective Synthesis of Nitrogen-Containing Compounds from Enamines J. Org. Chem. 2017, 82, 10968–10979. DOI
Ishikawa, H.; Nishino, H.; Nakajima, M.; Kotani, S. The 2016 kumamoto earthquake; reconstruction and countermeasures J. Synth. Org. Chem., Jpn. 2017, 75, 259–263. DOI
中島誠 ホスフィンオキシドを有機分子触媒とする不斉アルドール反応の開発 化学工業 2017, 68, 66–72.
Alim, N. R.; Miyazaki, S.; Shimoda, Y.; Sugiura, M.; Nakajima, M.; Kotani, S. Asymmetric aldol/vinylogous aldol/cyclization reaction using phosphine oxide catalysts Chem. Pharm. Bull. 2017, 65, 989–993. DOI
Kotani, S.; Kai, K.; Sugiura, M.; Nakajima, M. Sequential Catalysis of Phosphine Oxide for Stereoselective Synthesis of Stereopentads Org. Lett. 2017, 19, 3672–3675. DOI

2016(6)

Kotani, S.; Asano, T.; Moritani, M.; Nakajima, M. Enantioselective amination of acyclic α-alkylated β-keto esters catalyzed by chiral lithium binaphtholate Tetrahedron Lett. 2016, 57, 4217–4219. DOI
Kotani, S.; Miyazaki, S.; Kawahara, K.; Shimoda, Y.; Sugiura, M.; Nakajima, M. Stereoselective Synthesis of Highly Functionalized 2,3-Dihydro-4-pyranones Using Phosphine Oxide as Catalyst Chem. Pharm. Bull. 2016, 64, 189–192. DOI
Sakamoto, M.; Kaneko, T.; Orito, Y.; Nakajima, M. Enantioselective Michael Addition of a Malonate Ester Synlett 2016, 27, 2477–2780.
Osakama, K.; Nakajima, M. Asymmetric Direct 1,2-Addition of Aryl Grignard Reagents to Aryl Alkyl Ketones Org. Lett. 2016, 18, 236–239. DOI
Kotani, S.; Kai, K.; Shimoda, Y.; Hu, H.; Gao, S.; Sugiura, M.; Ogasawara, M.; Nakajima, M. Concise Asymmetric Construction of C2-Symmetric 1,9-Diarylnonanoids Using a Hypervalent Silicon Complex: Total Synthesis of (−)-Ericanone Chem. Asian J. 2016, 11, 376–379. DOI
Enoki, Y.; Watanabe, H.; Arake, R.; Sugimoto, R.; Imafuku, T.; Tominaga, Y.; Ishima, Y.; Kotani, S.; Nakajima, M.; Tanaka, M.; Matsushita, K.; Fukagawa, M.; Otagiri, M.; Maruyama, T. Indoxyl sulfate potentiates skeletal muscle atrophy by inducing the oxidative stress-mediated expression of myostatin and atrogin-1 Sci. Rep. 2016, 6, 32084. DOI

2015(8)

Ishima, Y.; Narisoko, T.; Kragh-Hansen, U.; Kotani, S.; Nakajima, M.; Otagiri, M.; Maruyama, T. Nitration of indoxyl sulfate facilitates its cytotoxicity in human renal proximal tubular cells via expression of heme oxygenase-1 Biochem. Biophys. Res. Commun. 2015, 465, 481–487. DOI
Kotani, S.; Sakamoto, M.; Osakama, K.; Nakajima, M. A Sterically Congested α-Cyanoamine as a Cyanating Reagent: Cyanation of Acetals and Orthoesters Eur. J. Org. Chem. 2015, 2015, 6606–6609. DOI
Ohura, K.; Nakada, Y.; Kotani, S.; Imai, T. Design of fexofenadine prodrugs based on tissue-specific esterase activity and their dissimilar recognition by p-glycoprotein J. Pharm. Sci. 2015, 104, 3076–3083. DOI
Sugiura, M.; Ashigari, Y.; Nakajima, M. One-Pot Synthesis of β,β-Disubstituted α,β-Unsaturated Carbonyl Compounds J. Org. Chem. 2015, 80, 8830–8835. DOI
Sugiura, M.; Ishikawa, W.; Kuboyama, Y.; Nakajima, M. Conjugate Addition of Diboron Catalyzed by O-Monoacyltartaric Acid Synthesis 2015, 47, 2265–2269. DOI
Kotani, S.; Moritani, M.; Nakajima, M. Chiral Lithium Binaphtholate for Enantioselective Michael Addition of Acyclic α-Alkyl-β-Keto Esters to Vinyl Ketones Asian J. Org. Chem. 2015, 4, 616–618. DOI
Wada, Y.; Lee, H.; Hoshino, Y.; Kotani, S.; Shea, K. J.; Miura, Y. Design of multi-functional linear polymers that capture and neutralize a toxic peptide: a comparison with cross-linked nanoparticles J. Mater. Chem. B 2015, 3, 1706–1711. DOI
Watanabe, H.; Miyamoto, Y.; Enoki, Y.; Ishima, Y.; Kadowaki, D.; Kotani, S.; Nakajima, M.; Tanaka, M.; Matsushita, K.; Mori, Y.; Kakuta, T.; Fukagawa, M.; Otagiri, M.; Maruyama, T. p-Cresyl sulfate, a uremic toxin, causes vascular endothelial and smooth muscle cell damages by inducing oxidative stress Pharmacol. Res. Perspect. 2015, 3. DOI

2014(8)

Ito, M.; Kashiwagi, T.; Kotani, S.; Nakajima, M.; Sugiura, M. Imino ene-type reaction of enamines with N-sulfonylimines and application to diastereoselective synthesis of N-sulfonyl-1,3-diamines Tetrahedron Lett. 2014, 55, 4082–4085. DOI
Kashiwagi, T.; Kotani, S.; Nakajima, M.; Sugiura, M. Diastereoselective synthesis of 1,3-diamines by a domino reaction of imines, enamines, and trichlorosilane Tetrahedron Lett. 2014, 55, 1924–1926. DOI
Kotani, S.; Kukita, K.; Tanaka, K.; Ichibakase, T.; Nakajima, M. Lithium Binaphtholate-Catalyzed Asymmetric Addition of Lithium Acetylides to Carbonyl Compounds J. Org. Chem. 2014, 79, 4817–4825. DOI
Osaka, Y.; Onimaru, H.; Kotani, S.; Kashiwagi, M.; Morisaki, H.; Takeda, J. The effects of doxapram on medullary respiratory neurones in brainstem-spinal cord preparations from newborn rats Anaesthesia 2014, 69, 468–475. DOI
Kotani, S.; Sugiura, M.; Nakajima, M. Enantioselective Double Aldol Reactions Involving the Sequential Activation of Silicon Tetrachloride by Chiral Phosphine Oxides Synlett 2014, 25, 631–640. DOI
Watanabe, H.; Sakaguchi, Y.; Sugimoto, R.; Kaneko, K.-I.; Iwata, H.; Kotani, S.; Nakajima, M.; Ishima, Y.; Otagiri, M.; Maruyama, T. Human organic anion transporters function as a high-capacity transporter for p-cresyl sulfate, a uremic toxin Clin. Exp. Nephrol. 2014, 18, 814–820. DOI
Kotani, S.; Aoki, S.; Sugiura, M.; Ogasawara, M.; Nakajima, M. Phosphine Oxide-Catalyzed Enantioselective Intramolecular Aldol Reaction via Regioselective Enolization of Unsymmetrical Diketones with Tetrachlorosilane Org. Lett. 2014, 16, 4802–4805. DOI
Sugiura, M.; Kinoshita, R.; Nakajima, M. O-Monoacyltartaric Acid Catalyzed Enantioselective Conjugate Addition of a Boronic Acid to Dienones: Application to the Synthesis of Optically Active Cyclopentenones Org. Lett. 2014, 16, 5172–5175. DOI

2013(7)

Kotani, S.; Ito, M.; Nozaki, H.; Sugiura, M.; Ogasawara, M.; Nakajima, M. Enantioselective Morita-Baylis-Hillman reaction catalyzed by a chiral phosphine oxide Tetrahedron Lett. 2013, 54, 6430–6433. DOI
Kotani, S.; Furusho, H.; Sugiura, M.; Nakajima, M. Facile synthesis of chiral 1,2-chlorohydrins via the ring-opening of meso-epoxides catalyzed by chiral phosphine oxides Tetrahedron 2013, 69, 3075–3081. DOI
Watanabe, H.; Miyamoto, Y.; Honda, D.; Tanaka, H.; Wu, Q.; Endo, M.; Noguchi, T.; Kadowaki, D.; Ishima, Y.; Kotani, S.; Nakajima, M.; Kataoka, K.; Kim-Mitsuyama, S.; Tanaka, M.; Fukagawa, M.; Otagiri, M.; Maruyama, T. p-Cresyl sulfate causes renal tubular cell damage by inducing oxidative stress by activation of NADPH oxidase Kidney Int. 2013, 83, 582–592. DOI
Kotani, S.; Sugiura, M.; Nakajima, M. Structure constructions utilizing continuous aldol reactions: deployment to stereoselective synthesis of polyols Kagaku (Kyoto) 2013, 68, 64–65.
Ogasawara, M.; Kotani, S.; Nakajima, H.; Furusho, H.; Miyasaka, M.; Shimoda, Y.; Wu, W.-Y.; Sugiura, M.; Takahashi, T.; Nakajima, M. Atropisomeric Chiral Dienes in Asymmetric Catalysis: C2-Symmetric (Z,Z)-2,3-Bis[1-(diphenylphosphinyl)ethylidene|tetralin as a Highly Active Lewis Base Organocatalyst Angew. Chem. Int. Ed. 2013, 52, 13798–13802. DOI
Shimoda, Y.; Kubo, T.; Sugiura, M.; Kotani, S.; Nakajima, M. Stereoselective synthesis of multiple stereocenters by using a double aldol reaction Angew. Chem. Int. Ed. 2013, 52, 3461–3464. DOI
Kotani, S.; Sugiura, M.; Nakajima, M. Enantioselective Aldol Reactions Catalyzed by Chiral Phosphine Oxides Chem. Rec. 2013, 13, 362–370. DOI

2012(8)

Osakama, K.; Sugiura, M.; Nakajima, M.; Kotani, S. Enantioselective reductive aldol reaction using tertiary amine as hydride donor Tetrahedron Lett. 2012, 53, 4199–4201. DOI
Ichibakase, T.; Kaneko, T.; Orito, Y.; Kotani, S.; Nakajima, M. Construction of quaternary carbon centers by a base-catalyzed enantioselective aldol reaction and related reactions of trimethoxysilyl enol ethers Tetrahedron 2012, 68, 4210–4224. DOI
Kotani, S.; Nakajima, M. C-X bond formation: organocatalytic enantioselective halogenation of meso epoxides Comprehensive Chirality 2012, 506. DOI
Aoki, S.; Kotani, S.; Sugiura, M.; Nakajima, M. Trichlorosilyl triflate-mediated enantioselective directed cross-aldol reaction between ketones using a chiral phosphine oxide as an organocatalyst Chem. Commun. 2012, 48, 5524–5526. DOI
Watanabe, H.; Noguchi, T.; Miyamoto, Y.; Kadowaki, D.; Kotani, S.; Nakajima, M.; Miyamura, S.; Ishima, Y.; Otagiri, M.; Maruyama, T. Interaction between two sulfate-conjugated uremic toxins, p-cresyl sulfate and indoxyl sulfate, during binding with human serum albumin Drug Metab. Dispos. 2012, 40, 1423–1428. DOI
Ohmaru, Y.; Sato, N.; Mizutani, M.; Kotani, S.; Sugiura, M.; Nakajima, M. Synthesis of aryl group-modified DIOP dioxides (Ar-DIOPOs) and their application as modular Lewis base catalysts Org. Biomol. Chem. 2012, 10, 4562–4570. DOI
Ichibakase, T.; Nakajima, M. Efficient Preparation of 1,3-Diol Derivatives with Three Contiguous Stereo-centers by an Enantioselective Direct Aldol-Tishchenko Reaction Synthesis 2012, 44, 3145–3151. DOI
Sugiura, M.; Nakajima, M. 6.8 Allylations of C-O and C-N Double Bonds and Related Reactions Comprehensive Chirality 2012, 6, 214–233. DOI

2011(8)

Kashiwagi, T.; Kotani, S.; Sugiura, M.; Nakajima, M. Synthesis of γ-amino alcohols from aldehydes, enamines, and trichlorosilane using Lewis base catalysts Tetrahedron 2011, 67, 531–539. DOI
Kotani, S.; Aoki, S.; Sugiura, M.; Nakajima, M. Trichlorosilyl triflate for enantioselective direct-type aldol reaction with chiral phosphine oxide Tetrahedron Lett. 2011, 52, 2834–2836. DOI
Tanaka, K.; Kukita, K.; Ichibakase, T.; Kotani, S.; Nakajima, M. Lithium acetylides as alkynylating reagents for the enantioselective alkynylation of ketones catalyzed by lithium binaphtholate Chem. Commun. 2011, 47, 5614–5616. DOI
Miyamoto, Y.; Watanabe, H.; Noguchi, T.; Kotani, S.; Nakajima, M.; Kadowaki, D.; Otagiri, M.; Maruyama, T. Organic anion transporters play an important role in the uptake of p-cresyl sulfate, a uremic toxin, in the kidney Nephrol. Dial. Transplant. 2011, 26, 2498–2502. DOI
Shimoda, Y.; Kotani, S.; Sugiura, M.; Nakajima, M. Enantioselective Double Aldol Reaction Catalyzed by Chiral Phosphine Oxide Chem. Eur. J. 2011, 17, 7992. DOI
Kotani, S.; Osakama, K.; Sugiura, M.; Nakajima, M. A Tertiary Amine as A Hydride Donor: Trichlorosilyl Triflate-mediated Conjugate Reduction of Unsaturated Ketones Org. Lett. 2011, 13, 3968–3971. DOI
Ichibakase, T.; Nakatsu, M.; Nakajima, M. Enantioselective Evans-Tishchenko Reduction of β-Hydroxyketone Catalyzed by Lithium Binaphtholate Molecules 2011, 16, 5008–5019. DOI
Ichibakase, T.; Nakajima, M. Direct Enantioselective Aldol-Tishchenko Reaction Catalyzed by Chiral Lithium Diphenylbinaphtholate Org. Lett. 2011, 13, 1579–1581. DOI

2010(11)

Oh, Y. S.; Kotani, S.; Sugiura, M.; Nakajima, M. Development of chiral dinitrones as modular Lewis base catalysts: asymmetric allylation of aldehydes with allyltrichlorosilanes Tetrahedron: Asymmetry 2010, 21, 1833–1835. DOI
Aoki, S.; Kotani, S.; Sugiura, M.; Nakajima, M. DMAP-catalyzed cyanation of aldehydes and ketones with ethyl cyanoformate Tetrahedron Lett. 2010, 51, 3547–3549. DOI
Nakamura, Y.; Burke, A. M.; Kotani, S.; Ziller, J. W.; Rychnovsky, S. D. Total Synthesis of (-)-Lycoperine A Org. Lett. 2010, 12, 72–75. DOI
Sugiura, M.; Sato, N.; Sonada, Y.; Kotani, S.; Nakajima, M. Diastereo- and enantioselective reductive aldol reaction with trichlorosilane using chiral Lewis bases as organocatalysts Chem. Asian J. 2010, 5, 478–481. DOI
Matsunaga, H.; Tokuda, R.; Nakajima, M.; Ishizuka, T. Sterically congested, "roofed" β-iminodisulfides as new chiral ligands for palladium-catalyzed, asymmetric allylic alkylation Chem. Pharm. Bull. 2010, 58, 1419–1421. DOI
Ueda, T.; Tanaka, K.; Ichibakase, T.; Orito, Y.; Nakajima, M. Enantioselective alkynylation of carbonyl compounds with trimethoxysilylalkynes catalyzed by lithium binaphtholate Tetrahedron 2010, 66, 7726–7731. DOI
Tanaka, K.; Ueda, T.; Ichibakase, T.; Nakajima, M. Enantioselective alkynylation of ketones with trimethoxysilylalkynes using lithium binaphtholate as a catalyst Tetrahedron Lett. 2010, 51, 2168–2169. DOI
中島誠 有機オキシド化合物を触媒とする直接的不斉アルドール反応の開発 化学工業 2010, 61, 662–666.
Sugiura, M.; Tokudomi, M.; Nakajima, M. Enantioselective conjugate addition of boronic acids to enones catalyzed by O-monoacyltartaric acids Chem. Commun. 2010, 46, 7799–7800. DOI
中島誠 第四級不斉炭素を構築するアルドール反応 『使える！有機合成反応241実践ガイド』（化学同人） 2010, 248–249.
杉浦正晴; 中島誠 エノンの不斉還元的アルドール反応 『使える！有機合成反応241実践ガイド』（化学同人） 2010, 472–473.

2009(5)

Kotani, S.; Shimoda, Y.; Sugiura, M.; Nakajima, M. Novel enantioselective direct aldol-type reaction promoted by a chiral phosphine oxide as an organocatalyst Tetrahedron Lett. 2009, 50, 4602–4605. DOI
Shimoda, Y.; Tando, T.; Kotani, S.; Sugiura, M.; Nakajima, M. Enantioselective aldol reaction of silyl ketene acetals promoted by a Lewis base-activated Lewis acid catalyst Tetrahedron: Asymmetry 2009, 20, 1369–1370. DOI
Sugiura, M.; Kumahara, M.; Nakajima, M. Asymmetric synthesis of 4H-1,3-oxazines: Enantioselective reductive cyclization of N-acylated β-amino enones with trichlorosilane catalyzed by chiral Lewis bases Chem. Commun. 2009, 3585–3587. DOI
Matsunaga, H.; Nakanishi, K.; Nakajima, M.; Kunieda, T.; Ishizuka, T. A chiral "roofed" cis-diamine-Ru(II) complex: An efficient catalyst for asymmetric transfer hydrogenation of ketimines Heterocycles 2009, 78, 617–622. DOI
中島誠 クロロシリル化合物を活性化する塩基触媒による不斉合成反応 『フロンティア21 進化を続ける有機触媒』（化学同人） 2009, 131–136.

2008(3)

Nakanishi, K.; Kotani, S.; Sugiura, M.; Nakajima, M. First asymmetric Abramov-type phosphonylation of aldehydes with trialkyl phosphites catalyzed by chiral Lewis bases Tetrahedron 2008, 64, 6415–6419. DOI
Sugiura, M.; Sato, N.; Kotani, S.; Nakajima, M. Lewis base-catalyzed conjugate reduction and reductive aldol reaction of α,β-unsaturated ketones using trichlorosilane Chem. Commun. 2008, 4309–4311. DOI
Ichibakase, T.; Orito, Y.; Nakajima, M. Enantioselective construction of quaternary asymmetric carbon centers using an aldol reaction of trimethoxysilyl enol ethers catalyzed by lithium binaphtholate Tetrahedron Lett. 2008, 49, 4427–4429. DOI

2007(3)

Kotani, S.; Hashimoto, S.; Nakajima, M. Chiral phosphine oxide BINAPO as a Lewis base catalyst for asymmetric allylation and aldol reaction of trichlorosilyl compounds Tetrahedron 2007, 63, 3122–3132. DOI
Kida, A.; Kakihana, K.; Kotani, S.; Kurosu, T.; Miura, O. Glycogen synthase kinase-3β and p38 phosphorylate cyclin D2 on Thr280 to trigger its ubiquitin/proteasome-dependent degradation in hematopoietic cells Oncogene 2007, 26, 6630–6640. DOI
Tsutsui, H.; Shimada, N.; Abe, T.; Anada, M.; Nakajima, M.; Nakamura, S.; Nambu, H.; Hashimoto, S. Catalytic enantioselective tandem carbonyl ylide formation/1,3 dipolar cycloaddition reactions of α-diazo ketones with aromatic aldehydes using dirhodium(II) tetrakis[N-benzene-fusedphthaloyl- (S)-valinate] Adv. Synth. Catal. 2007, 349, 521–526. DOI

2006(5)

Kotani, S.; Yamauchi, T.; Teramoto, T.; Ogura, H. Pharmacological evidence of cholinergic involvement in adult hippocampal neurogenesis in rats Neuroscience 2006, 142, 505–514. DOI
Kotani, S.; Hashimoto, S.; Nakajima, M. Enantioselective aldol reactions of trichlorosilyl enol ethers catalyzed by the chiral phosphine oxide BINAPO Synlett 2006, 1116–1118. DOI
Orito, Y.; Hashimoto, S.; Ishizuka, T.; Nakajima, M. Chiral Base-Catalyzed Aldol Reaction of Trimethoxysilyl Enol Ethers: Effect of Water as an Additive on Stereoselectivities Tetrahedron 2006, 62, 390. DOI
Orito, Y.; Nakajima, M. Lewis base catalyzed asymmetric reactions involving hypervalent silicate intermediates Synthesis 2006, 1391–1401. DOI
中島誠 N-オキシド・ホスフィンオキシドを触媒とする不斉合成反応 『有機分子触媒の新展開』（シーエムシー出版） 2006, 59–70.

2005(3)

Nakajima, M.; Kotani, S.; Ishizuka, T.; Hashimoto, S. Chiral phosphine oxide BINAPO as a catalyst for enantioselective allylation of aldehydes with allyltrichlorosilanes Tetrahedron Lett. 2005, 46, 157–159. DOI
Tokuoka, E.; Kotani, S.; Matsunaga, H.; Ishizuka, T.; Hashimoto, S.; Nakajima, M. Asymmetric ring opening of meso-epoxides catalyzed by the chiral phosphine oxide BINAPO Tetrahedron: Asymmetry 2005, 16, 2391–2392. DOI
Yamakuchi, M.; Matsunaga, H.; Tokuda, R.; Ishizuka, T.; Nakajima, M.; Kunieda, T. Sterically congested 'roofed' 2-thiazolines as new chiral ligands for copper(II)-catalyzed asymmetric Diels-Alder reactions Tetrahedron Lett. 2005, 46, 4019–4022. DOI

2004(4)

Nakajima, M.; Orito, Y.; Ishizuka, T.; Hashimoto, S. Enantioselective aldol reaction of trimethoxysilyl enol ether catalyzed by lithium binaphtholate Org. Lett. 2004, 6, 3763–3765. DOI
中島誠 ルイス塩基として機能する不斉有機触媒 化学と工業 2004, 57, 720–723.
Anada, M.; Washio, T.; Shimada, N.; Kitagaki, S.; Nakajima, M.; Shiro, M.; Hashimoto, S. A new dirhodium(II) carboxamidate complex as a chiral lewis acid catalyst for enantioselective hetero-Diels-Alder reactions Angew. Chem. Int. Ed. 2004, 43, 2665–2668. DOI
Nakajima, M.; Yokota, T.; Saito, M.; Hashimoto, S. Enantioselective aldol reactions of trichlorosilyl enol ethers catalyzed by chiral N,N'-dioxides and monodentate N-oxides Tetrahedron Lett. 2004, 45, 61–64. DOI

2003(3)

Hikichi, K.; Kitagaki, S.; Anada, M.; Nakamura, S.; Nakajima, M.; Shiro, M.; Hashimoto, S. Synthesis and evaluation of novel dirhodium(II) carboxylate catalysts with atropisomeric biaryl backbone Heterocycles 2003, 61, 391.
Nakajima, M. Chiral N-oxides as catalysts or ligands in enantioselective reactions J. Synth. Org. Chem., Jpn. 2003, 61, 1081–1087. DOI
Nakajima, M.; Yamamoto, S.; Yamaguchi, Y.; Nakamura, S.; Hashimoto, S. Enantioselective Michael additions of β-keto esters to α,β-unsaturated carbonyl compounds catalyzed by a chiral biquinoline N,N'-dioxide-scandium trifluoromethanesulfonate complex Tetrahedron 2003, 59, 7307–7313. DOI

2002(3)

Nakamura, S.; Inagaki, J.; Kudo, M.; Sugimoto, T.; Obara, K.; Nakajima, M.; Hashimoto, S. Studies directed toward the total synthesis of pinnatoxin A: synthesis of the 6,5,6-dispiroketal (BCD ring) system by double hemiketal formation/hetero-Michael addition strategy Tetrahedron 2002, 58, 10353–10374. DOI
Nakajima, M.; Saito, M.; Uemura, M.; Hashimoto, S. Enantioselective ring opening of meso-epoxides with tetrachlorosilane catalyzed by chiral bipyridine N,N'-dioxide derivatives Tetrahedron Lett. 2002, 43, 8827–8829. DOI
Nakajima, M.; Saito, M.; Hashimoto, S. Selective synthesis of optically active allenic and homopropargylic alcohols from propargyl chloride Tetrahedron: Asymmetry 2002, 13, 2449–2452. DOI

2001(6)

Nakamura, S.; Inagaki, J.; Sugimoto, T.; Kudo, M.; Nakajima, M.; Hashimoto, S. A stereoselective synthesis of the C10-C31 (BCDEF ring) portion of pinnatoxin A Org. Lett. 2001, 3, 4075–4078. DOI
Kitagaki, S.; Yanamoto, Y.; Tsutsui, H.; Anada, M.; Nakajima, M.; Hashimoto, S. Enantioselective [2,3]-sigmatropic and [1,2]-Stevens rearrangements via intramolecular formation of allylic oxonium ylides catalyzed by chiral dirhodium(II) carboxylates (vol 42, pg 6361, 2001) Tetrahedron Lett. 2001, 42, 7715. DOI
Takahashi, T.; Tsutsui, H.; Tamura, M.; Kitagaki, S.; Nakajima, M.; Hashimoto, S. Catalytic asymmetric synthesis of 1,1'-spirobi[indan-3,3'-dione] via a double intramolecular C-H insertion process Chem. Commun. 2001, 1604–1605. DOI
Nakajima, M.; Yamaguchi, Y.; Hashimoto, S. Enantioselective Michael addition of β-keto esters to methyl vinyl ketone employing a chiral N,N'-dioxide-scandium trifluoromethanesulfonate complex as a catalyst Chem. Commun. 2001, 1596–1597. DOI
Kitagaki, S.; Yanamoto, Y.; Okubo, H.; Nakajima, M.; Hashimoto, S. Enantiocontrol in tandem allylic sulfonium ylide generation and [2,3] sigmatropic rearrangement catalyzed by chiral dirhodium(II) complexes Heterocycles 2001, 54, 623.
Tsutsui, H.; Matsuura, M.; Makino, K.; Nakamura, S.; Nakajima, M.; Kitagaki, S.; Hashimoto, S. Enantioselective tandem formation and [2,3]-sigmatropic rearrangement of cyclic propargylic oxonium ylides catalyzed by dirhodium(II) tetrakis[N-phthaloyl-(S)-tert-leucinate] Isr. J. Chem. 2001, 41, 283–295.

2000(5)

Saito, M.; Nakajima, M.; Hashimoto, S. Enantioselective conjugate addition of thiols to cyclic enones and enals catalyzed by chiral N,N'-dioxide-cadmium iodide complex Tetrahedron 2000, 56, 9589–9594. DOI
Kitagaki, S.; Yasugahira, M.; Anada, M.; Nakajima, M.; Hashimoto, S. Enantioselective intermolecular 1,3-dipolar cycloaddition via ester-derived carbonyl ylide formation catalyzed by chiral dirhodium(II) carboxylates Tetrahedron Lett. 2000, 41, 5931–5935. DOI
Nakajima, M.; Saito, M.; Hashimoto, S. One-pot enantioselective synthesis of optically active homoallylic alcohols from allyl halides Chem. Pharm. Bull. 2000, 48, 306–307. DOI
Nakajima, M. Chiral Lewis Base-Catalyed Reactions Involving Hypervalent Silicates J. Synth. Org. Chem., Jpn. 2000, 58, 839–847. DOI
Nakajima, M. Synthesis and application of novel biaryl compounds with axial chirality as catalysts in enantioselective reactions Yakugaku Zasshi 2000, 120, 68–75. DOI

1999(4)

Inagaki, J.; Sakamoto, H.; Nakajima, M.; Nakamura, S.; Hashimoto, S. A facile synthesis of 3'-deoxy-3'-fluorothymidine via a highly stereoselective glycosylation with 2,3-dideoxy-3-fluoro-D-erythro-pentofuranosyl diethyl phosphite Synlett 1999, 1274–1276.
Tanaka, H.; Sakamoto, H.; Sano, A.; Nakamura, S.; Nakajima, M.; Hashimoto, S. An extremely mild and stereocontrolled construction of 1,2-cis-α-glycosidic linkages via benzyl-protected glycopyranosyl diethyl phosphites Chem. Commun. 1999, 1259–1260. DOI
Anada, M.; Sugimoto, T.; Watanabe, N.; Nakajima, M.; Hashimoto, S. A concise synthesis of (+)-α-allokainic acid via site- and diastereoselective intramolecular C-H insertion process Heterocycles 1999, 50, 969–980. DOI
Nakajima, M.; Miyoshi, I.; Kanayama, K.; Hashimoto, S.; Noji, M.; Koga, K. Enantioselective synthesis of binaphthol derivatives by oxidative coupling of naphthol derivatives catalyzed by chiral diamine copper complexes J. Org. Chem. 1999, 64, 2264–2271. DOI

1998(4)

Nakajima, M.; Hashimoto, S.; Noji, M.; Koga, K. Aerobic oxidative coupling of 2-naphthol derivatives catalyzed by a copper-amine complex without solvent Chem. Pharm. Bull. 1998, 46, 1814–1815. DOI
Nakajima, M.; Saito, M.; Shiro, M.; Hashimoto, S. (S)-3,3'-dimethyl-2,2'-biquinoline N,N'-dioxide as an efficient catalyst for enantioselective addition of allyltrichlorosilanes to aldehydes J. Am. Chem. Soc. 1998, 120, 6419–6420. DOI
Murakata, M.; Yasukata, T.; Aoki, T.; Nakajima, M.; Koga, K. Stereoselective reactions. 30. Enantioselective alkylation of the lithium enolates of six-membered cyclic ketones using tetradentate chiral amines in the presence of lithium bromide Tetrahedron 1998, 54, 2449–2458. DOI
Nakajima, M.; Sasaki, Y.; Iwamoto, H.; Hashimoto, S. Bipyridine N,N'-dioxide: A felicitous ligand for methyltrioxorhenium-catalyzed epoxidation of olefins with hydrogen peroxide Tetrahedron Lett. 1998, 39, 87–88. DOI

1997(4)

Hashimoto, S.; Inagaki, J.; Sakamoto, H.; Sano, A.; Nakajima, M. N-glycosylation with glycosyl diethyl phosphites: A highly stereoselective synthesis of 2'-deoxy-β-ribonucleosides Heterocycles 1997, 46, 215–220. DOI
Chatani, H.; Nakajima, M.; Kawasaki, K.; Koga, K. Chiral bidentate lithium amides having a chiral amide nitrogen for enantioselective deprotonation of 4-tert-butylcycloxexanone Heterocycles 1997, 46, 53–56.
Nakajima, M.; Sasaki, Y.; Shiro, M.; Hashimoto, S. A novel axially dissymmetric chiral ligand based on amine N-oxide: (R)- and (S)-3,3'-dimethyl-2,2'-biquinoline N,N'-dioxide Tetrahedron: Asymmetry 1997, 8, 341–344. DOI
中島誠 軸不斉配位子ビナフトールの新合成法の開発 道薬誌 1997, 14, 6.

1996(1)

橋本俊一; 中島誠 オリゴ糖鎖合成の新戦略 ファルマシア 1996, 32, 1375–1380.

1995(5)

Hashimoto, S.; Sano, A.; Umeo, K.; Nakajima, M.; Ikegami, S. An extremely mild and general method for the construction of 1,2-trans-β-glycosidic linkages via glycopyranosyl diethyl phosphites with participating groups at C-2 Chem. Pharm. Bull. 1995, 43, 2267–2269. DOI
Hashimoto, S.; Sano, A.; Sakamoto, H.; Nakajima, M.; Yanagiya, Y.; Ikegami, S. An attempt at the direct construction of 2-deoxy-β-glycosidic linkages capitalizing on 2-deoxyglycopyranosyl diethyl phosphites as glycosyl donors Synlett 1995, 1271. DOI
Nakajima, M.; Kanayama, K.; Miyoshi, I.; Hashimoto, S. Catalytic asymmetric synthesis of binaphthol derivatives by aerobic oxidative coupling of 3-hydroxy-2-naphthoates with chiral diamine-copper complex Tetrahedron Lett. 1995, 36, 9519–9520. DOI
Hashimoto, S.; Honda, T.; Yanagiya, Y.; Nakajima, M.; Ikegami, S. Highly selective glycosidation reactions capitalizing on phosphorus-containing leaving groups J. Synth. Org. Chem., Jpn. 1995, 53, 620–632.
Hashimoto, S.; Umeo, K.; Sano, A.; Watanabe, N.; Nakajima, M.; Ikegami, S. An extremely mild and stereocontrolled construction of 1,2-trans-β-glycosidic linkages capitalizing on benzyl-protected glycopyranosyl diethyl phosphites as glycosyl donors Tetrahedron Lett. 1995, 36, 2251–2254. DOI

1994(2)

Noji, M.; Nakajima, M.; Koga, K. A new catalytic system for aerobic oxidative coupling of 2-naphthol derivatives by the use of CuCl–amine complex: a practical synthesis of binaphthol derivatives Tetrahedron Lett. 1994, 35, 7983–7984. DOI
Kumamoto, T.; Aoki, S.; Nakajima, M.; Koga, K. Chiral lithium 2-aminoalkoxides as reagents for enantioselective michael reaction Tetrahedron: Asymmetry 1994, 5, 1431–1432. DOI

1993(7)

Kubota, H.; Nakajima, M.; Koga, K. Enantioselective palladium-catalyzed allylic alkylation with C2-symmetrical chiral diamine ligands Tetrahedron Lett. 1993, 34, 8135–8138. DOI
Nakajima, M.; Tomioka, K.; Iitaka, Y.; Koga, K. Highly enantioselective dihydroxylation of olefins by osmium tetroxide with chiral diamines Tetrahedron 1993, 49, 10793–10806. DOI
Nakajima, M.; Tomioka, K.; Koga, K. Short-step asymmetric syntheses of anthracycline antibiotics via enantioselective dihydroxylation by osmium tetroxide with a chiral diamine Tetrahedron 1993, 49, 10807–10816. DOI
Nakajima, M.; Tomioka, K.; Koga, K. Design and synthesis of novel chiral pyrrolidine-based diamines with C2-symmetry Tetrahedron 1993, 49, 9735–9750. DOI
Nakajima, M.; Tomioka, K.; Koga, K. Enantioselective 1,2-addition of Grignard reagents to aldehydes using chiral diamines Tetrahedron 1993, 49, 9751–9758. DOI
Aoki, K.; Nakajima, M.; Tomioka, K.; Koga, K. Reinvestigation on the optical purities of optically active trimethylsilyl enol ethers of 4-substituted cyclohexanones Chem. Pharm. Bull. 1993, 41, 994–996. DOI
中島誠 レニウムを用いた酸化的環化反応 ファルマシア 1993, 29, 785.

1992(1)

Still, W.; Kilburn, J.; Sanderson, P.; Liu, R.; Wiley, M.; Hollinger, F.; Hawley, R.; Nakajima, M.; Bernardi, A.; Hong, J.; Namgoong, S. Enantioselective hosts for neutral derivatives of amino acids Isr. J. Chem. 1992, 32, 41–45.

1990(5)

Murakata, M.; Nakajima, M.; Koga, K. Enantioselective alkylation at the α-position of cyclic ketones using a chiral lithium amide as a base in the presence of lithium bromide J. Chem. Soc., Chem. Commun. 1990, 1657–1658. DOI
Tomioka, K.; Shinmi, Y.; Shiina, K.; Nakajima, M.; Koga, K. Stereoselective reactions. 19. asymmetric dihydroxylation of olefins by employing osmium tetroxide-chiral amine complexes Chem. Pharm. Bull. 1990, 38, 2133–2135. DOI
Kim, H.; Shirai, R.; Kawasaki, H.; Nakajima, M.; Koga, K. Enantioselective deprotonation of the meso forms of 2,6-dimethylcyclohexanone and 3,5-dimethylcyclohexanones Heterocycles 1990, 30, 307–310. DOI
Sobukawa, M.; Nakajima, M.; Koga, K. Regioselective enolization of optically active 3-keto steroids using chiral lithium amides Tetrahedron: Asymmetry 1990, 1, 295–298. DOI
Tomioka, K.; Nakajima, M.; Koga, K. Dramatic enantioselectivity change in dihydroxylation of olefins with chiral amine-osmium tetroxide complex Tetrahedron Lett. 1990, 31, 1741–1742. DOI

1989(3)

Tomioka, K.; Nakajima, M.; Koga, K. A short asymmetric synthesis of anthracycline antibiotics J. Chem. Soc., Chem. Commun. 1989, 1921–1922. DOI
Kim, H.; Kawasaki, H.; Nakajima, M.; Koga, K. Kinetic resolution of racemic 2-substituted cyclohexanones by enantioselective deprotonation Tetrahedron Lett. 1989, 30, 6537–6540. DOI
Nakajima, M.; Tomioka, K.; Koga, K. Asymmetric Oxidation of Olefins with Osmium Tetroxide J. Synth. Org. Chem., Jpn. 1989, 47, 878–888. DOI

1988(1)

Tomioka, K.; Nakajima, M.; Iitaka, Y.; Koga, K. Mechanistic aspects of asymmetric cis-dihydroxylation of olefins with osmium tetroxide employing a C2-symmetric chiral diamine Tetrahedron Lett. 1988, 29, 573–576. DOI

1987(4)

Tomioka, K.; Nakajima, M.; Koga, K. Enantioface differentiation in cis dihydroxylation of C=C double-bonds by osmium tetroxide with use of a chiral diamine with D2 symmetry J. Am. Chem. Soc. 1987, 109, 6213–6215. DOI
Tomioka, K.; Nakajima, M.; Koga, K. Novel use of aryloxyaluminum dichloride in the chiral diamine mediated asymmetric addition reaction of Grignard reagents to benzaldehyde Tetrahedron Lett. 1987, 28, 1291–1292. DOI
中島誠; 富岡清; 古賀憲司四酸化オスミウムを用いたオレフィンの不斉酸化反応化学 1987, 42, 422–423.
Tomioka, K.; Nakajima, M.; Koga, K. Novel 3,4-diarylpyrrolidine-based chiral ligands for the asymmetric reaction of arylmagnesium bromides with aldehydes Chem. Lett. 1987, 65–68. DOI