Laboratory for Organic Synthesis & Catalysis, Ooilab Publications

Site Map ・ Access

原著論文 : Original Papers

102.

Excited-state tris(pentafluorophenyl)borane as a strong single-electron oxidant: Photophysical properties and catalysis

Yoshitaka Aramaki, Yuki Uchida, Ryo Ishikawa, and Takashi Ooi

J. Photochem. Photobio. 2023, 18, 100206.

DOI: 10.1016/j.jpap.2023.100206

101.

Catalytic Formal Carbyne Transformation of Phosphorus Ylides

Ryuhei Suzuki, Taiga Ando, Fritz Deufel, Kohsuke Ohmatsu, and Takashi Ooi

ChemRxiv 2023
DOI: 10.26434/chemrxiv-2023-mx0vg

100.

Zwitterionic Diphenylphosphinyl Amidate as a Powerful Photoinduced Hydrogen-Atom-Transfer Catalyst for C-H Alkylation of Simple Alkanes

Kohsuke Ohmatsu, Ryuhei Suzuki, Hiroki Fujira, and Takashi Ooi

J. Org. Chem. 2023, 88, 6553-6556.

DOI: 10.1021/acs.joc.2c02362

99.

Hydrogen-Atom Transfer Catalysis for C-H Alkylation of Benzylic Fluorides

Kohsuke Ohmatsu, Hiroki Fujita, Ryuhei Suzuki, and Takashi Ooi

Org. Lett. 2022, 24, 3134-3137.

DOI: 10.1021/acs.orglett.2c00817
98.

Thioamidate Ion as Effective Cocatalyst for Photoinduced C-H Alkylation via Multisite Proton-coupled Electron Transfer

Kohsuke Ohmatsu, Haruka Fujimori, Kodai Minami, Kosuke Nomura, Mari Kiyokawa, and Takashi Ooi

Chem. Lett. 2022, 51, 445-447.

DOI: 10.1246/cl.220026
97.

In Silico Analysis and Synthesis of Nafamostat Derivatives and Evaluation of Their Anti-SARS-CoV-2 Activity

Kazuhiro J. Fujimoto, Daniel C. F. Hobbs, Miki Umeda, Akihiro Nagata, Rie Yamaguchi, Yoshitaka Sato, Ayato Sato, Kohsuke Ohmatsu, Takashi Ooi, Takeshi Yanai, Hiroshi Kimura, Takayuki Murata

Viruses 2022, 14, 389.

DOI: 10.3390/v14020389
96.

Hydrogen-Atom-Transfer-Mediated Acceptorless Dehydrogenative Cross-Coupling Enabled by Multiple Catalytic Functions of Zwitterionic Triazolium Amidate

Kodai Minami, Kohsuke Ohmatsu, and Takashi Ooi

ACS Catal. 2022, 12, 1971

DOI: 10.1021/acscatal.1c05604
95.

Catalytic Asymmetric Strecker Reaction of Ketoimines with Potassium Cyanide

Kohsuke Ohmatsu, Yusuke Morita, Mari Kiyokawa, Kimihiro Hoshino, and Takashi Ooi

Asian J. Org. Chem. 2021, 10, 3237-3240

DOI: 10.1002/ajoc.202100608
94.

o-Quinone methide with overcrowded olefinic core as a catalytically-active surrogate of triarylmethylium salt for dehydridative oxidationof benzylic alcohols under aerobic photoirradiation conditions

Kohsuke Kato, Daisuke Uraguchi, and Takashi Ooi

Tetrahedron 2021, 100, 132459

DOI: 10.1016/j.tet.2021.132459
93. Catalytic Asymmetric Cyanoalkylation of Electron-Deficient Olefins with Potassium Cyanide and Alkyl Halides Kohsuke Ohmatsu, Yusuke Morita, Mari Kiyokawa, and Takashi Ooi J. Am. Chem. Soc. 2021, 143, 11218-11224 DOI: 10.1021/jacs.1c05380

92. Synthesis and enantioseparation of chiral Au₁₃ nanoclusters protected by bis-N-heterocyclic carbene ligands Hong Yi, Kimberly M. Osten, Tetyana I. Levchenko, Alex J. Veinot, Yoshitaka Aramaki, Takashi Ooi, Masakazu Nambo, and Cathleen M. Crudden Chem. Sci. 2021, 12, 10436-10440 DOI: 10.1039/D1SC03076K
91. Exploiting Transient Radical Cations as Brønsted Acids for Allylic C-H Heteroarylation of Enol Silyl Ethers Tsubasa Nakashima, Haruka Fujimori, Kohsuke Ohmatsu, and Takashi Ooi Chem. Eur. J. 2021, 27, 9253-9256 DOI: 10.1002/chem.202101352
90. Catalytic Asymmetric Synthesis of 5-Membered Alicyclic α-Quaternary β-Amino Acids via [3+2]-Photocycloaddition of α-Substituted Acrylates Yuto Kimura, Daisuke Uraguchi and Takashi Ooi Org. Biomol. Chem. 2021, 19, 1744-1747 DOI: 10.1039/D1OB00126D
89.

o-Quinone Methide with Overcrowded Olefin Component as a Dehydridation Catalyst under Aerobic Photoirradiation Conditions

Daisuke Uraguchi, Kohsuke Kato, and Takashi Ooi

Chem. Sci. 2021, 12, 2778-2783

DOI: 10.1039/D0SC06240E

Selected as a "front cover"
88.

Urea as a Redox-Active Directing Group under Asymmetric Photocatalysis of Iridium-Chiral Borate Ion Pairs

Daisuke Uraguchi, Yuto Kimura, Fumito Ueoka, and Takashi Ooi

J. Am. Chem. Soc. 2020, 142, 19462-19467

DOI: 10.1021/jacs.0c09468

Selected as a "front cover"
87. Hybrid Catalysis of 8-Quinolinecarboxaldehyde and Br?nsted Acid for Efficient Racemization of α-Amino Amides and Its Application in Chemoenzymatic Dynamic Kinetic Resolution Kohsuke Ohmatsu, Mari Kiyokawa, Yuto Shirai, Yuya Nagato, and Takashi Ooi HETEROCYCLES 2021, 103, 218-224 DOI: 10.3987/COM-20-S(K)32
86.

Mannich-type allylic C-H functionalization of enol silyl ethers under photoredox-thiol hybrid catalysis

Tsubasa Nakashima, Kohsuke Ohmatsu, Takashi Ooi

Org. Biomol. Chem. 2021, 19, 141-145

DOI: 10.1039/D0OB01862G

Selected as a "outside front cover"
85. Ion-Paired Ligands for Palladium-Catalyzed Allylic Alkylation under Base-Free Conditions Kohsuke Ohmatsu, Naho Matsuyama, Yuya Nagato, and Takashi Ooi Chem. Lett. 2020, 49, 1114-1116 DOI: 10.1246/cl.200264
84.

Redox-Regulated Divergence in Photocatalytic Addition of α-Nitro Alkyl Radicals to Styrenes

Yuto Tsuchiya, Ryota Onai, Daisuke Uraguchi and Takashi Ooi

Chem. Commun. 2020, 56, 11014-11017

DOI: 10.1039/D0CC04821F

Selected as a "outside front cover"
83. A Structurally Robust Chiral Borate Ion: Molecular Design, Synthesis, and Asymmetric Catalysis Daisuke Uraguchi, Fumito Ueoka, Naoya Tanaka, Tomohito Kizu, Wakana Takahashi, Takashi Ooi Angew. Chem. Int. Ed. 2020, 59, 11456-11461 DOI: 10.1002/anie.202001637
82. Exploiting Single-Electron Transfer in Lewis Pairs for Catalytic Bond-Forming Reactions Yoshitaka Aramaki, Naoki Imaizumi, Mao Hotta, Jun Kumagai, and Takashi Ooi Chem. Sci. 2020, 11, 4305-4311 DOI: 10.1039/D0SC01159B
81. Non‐Enzymatic Hybrid Catalysis for Stereoconversion of l-Amino Acid Derivatives to d-Isomers Yuya Nagato, Mari Kiyokawa, Yusuke Ueki, Jun Kikuchi, Kohsuke Ohmatsu, Masahiro Terada, Takashi Ooi Asian J. Org. Chem. 2020, 9, 561-565 DOI: 10.1002/ajoc.202000067
80. Unveiling Latent Photoreactivity of Imines Daisuke Uraguchi, Yuto Tsuchiya, Tsuyoshi Ohtani, Takafumi Enomoto, Shigeyuki Masaoka, Daisuke Yokogawa, and Takashi Ooi Angew. Chem. Int. Ed. 2020, 59, 3665-3670 DOI: 10.1002/anie.201913555
79. Zwitterionic 1,2,3-Triazolium Amidate as a Catalyst for Photoinduced Hydrogen-Atom Transfer Radical Alkylation Kohsuke Ohmatsu, Ryuhei Suzuki, Yukino Furukawa, Makoto Sato, and Takashi Ooi ACS Catal. 2020, 10, 2627-2632 DOI: 10.1021/acscatal.9b04491
78. Inserting Nitrogen: An Effective Concept To Create Nonplanar and Stimuli-Responsive Perylene Bisimide Analogues Sakiho Hayakawa, Ayumi Kawasaki, Yongseok Hong, Daisuke Uraguchi, Takashi Ooi, Dongho Kim, Tomoyuki Akutagawa, Norihito Fukui, and Hiroshi Shinokubo J. Am. Chem. Soc. 2019, 141, 19807-19816 DOI: 10.1021/jacs.9b09556
77. Direct allylic C-H alkylation of enol silyl ethers enabled by photoredox-Brønsted base hybrid catalysis Kohsuke Ohmatsu, Tsubasa Nakashima, Makoto Sato, and Takashi Ooi Nat. Commun. 2019, 10, 2706 DOI: 10.1038/s41467-019-10641-y
76. Formal Hydroformylation of α,β-Unsaturated Carboxylic Acids under Photoexcited Ketone Catalysis Kailong Zhu, Tsuyoshi Ohtani, Chandra Bhushan Tripathi, Daisuke Uraguchi, and Takashi Ooi Chem. Lett. 2019, 48, 715-717 DOI: 10.1246/cl.190197
75.

Photocatalytic Borylcyclopropanation of α-Boryl Styrenes

Tsuyoshi Ohtani, Yuto Tsuchiya, Daisuke Uraguchi and Takashi Ooi

Org. Chem. Front. 2019, 6, 1734-1737

DOI: 10.1039/c9qo00197b

Selected as a "outside front cover"
74. A femto-molar range suicide germination stimulant for the parasitic plant Striga hermonthica Daisuke Uraguchi, Keiko Kuwata, Yuh Hijikata, Rie Yamaguchi, Hanae Imaizumi, Sathiyanarayanan AM, Christin Rakers, Narumi Mori, Kohki Akiyama, Stephan Irle, Peter McCourt, Toshinori Kinoshita, Takashi Ooi, Yuichiro Tsuchiya Science 2018, 362, 1301-1305 DOI: 10.1126/science.aau5445 プレスリリース (名古屋大学HP) 読売新聞, 朝日新聞, 中日新聞, 産経新聞, 時事通信(2018年12月14日), 毎日新聞（16日）, 日経産業新聞（18日）, 科学新聞（21日），現代化学2019年4月号（インタビュー）掲載 Highlighted in Synform 2019, A74-76. http://dx.doi.org/10.1055/s-0037-1612166 Highlighted in Science daily Highlighted in Alpha Galileo Highlighted in EurekAlert!
73.

Protonated Bis-1,2,3-triazole as an Anion-Binding Chiral Br&onsted Acid for Catalytic Asymmetric Friedel-Crafts Reaction of Indoles with Imines

Yukino Furukawa, Ryuhei Suzuki, Tsubasa Nakashima, Rafael Gramage-Doria, Kohsuke Ohmatsu, Takashi Ooi

Bull. Chem. Soc. J. 2018, 91, 1252-1257

DOI: 10.1246/bcsj.20180098

Selected as a "Supplementary Cover Art"
72.

Catalyst-Directed Guidance of Sulfur-Substituted Enediolates to Stereoselective Carbon-Carbon Bond Formation with Aldehydes

Daisuke Uraguchi, Kohei Yamada, Makoto Sato, and Takashi Ooi

J. Am. Chem. Soc. 2018, 140, 5110-5117

DOI: 10.1021/jacs.7b12949

Selected as a "Supplementary Cover Art"
71.

Catalyst-Enabled Site-divergent Stereoselective Michael Reactions: Overriding Intrinsic Reactivity of Enynyl Carbonyl Acceptors

Daisuke Uraguchi, Ryo Shibazaki, Naoya Tanaka, Kohei Yamada, Ken Yoshioka, and Takashi Ooi

Angew. Chem. Int. Ed. 2018, 57, 4732-4736

DOI: 10.1002/anie.201800057

Selected as a "Front Cover"

Selected as a "VIP"
70. Allenedicarboxylate as a Stereochemically Labile Electrophile for Chiral Organic Base-Catalyzed Stereoselective Michael Addition Daisuke Uraguchi, Yasutaka Kawai, Hitoshi Sasaki, Kohei Yamada, and Takashi Ooi Chem. Lett. 2018, 47, 594-597 DOI: 10.1246/cl.180031
69.

Molecular Design, Synthesis, and Asymmetric Catalysis of a Hexacoordinated Chiral Phosphate Ion

Daisuke Uraguchi, Hitoshi Sasaki, Yuto Kimura, Takaki Ito, and Takashi Ooi

J. Am. Chem. Soc. 2018, 140, 2765-2768

DOI: 10.1021/jacs.7b13433

Selected as a "Supplementary Cover Art"

プレスリリース (名古屋大学HP)
68.

Diastereo- and enantioselective phase-transfer alkylation of 3-substituted oxindoles with racemic secondary alkyl halides

Kohsuke Ohmatsu, Yukino Furukawa, Mari Kiyokawa and Takashi Ooi

Chem. Commun. 2017, 53, 13113-13116

DOI: 10.1039/C7CC07122A

Selected as a "Cover Picture"
67. Photoredox Ketone Catalysis for Direct C-H Imidation and Acyloxylation of Arenes Chandra Bhushan Tripathi, Tsuyoshi Ohtani, Michael T. Corbett and Takashi Ooi Chem. Sci. 2017, 8, 5622-5627 DOI: 10.1039/C7SC01700F
66. Determination of the absolute configuration of compounds bearing chiral quaternary carbon centers using the crystalline sponge method Shiho Sairenji, Takashi Kikuchi, Mohamed Ahmed Abozeid, Shinobu Takizawa, Hiroaki Sasai, Yuichiro Ando, Kohsuke Ohmatsu, Takashi Ooi and Makoto Fujita Chem. Sci. 2017, 8, 5132-5136 DOI: 10.1039/c7sc01524k
65.

N-Sulfonyl α-Imino Ester-Derived Chiral Oxaziridines: Catalytic Asymmetric Synthesis and Application as a Modular Chiral Organic Oxidant

Naoya Tanaka, Ryosuke Tsutsumi, Daisuke Uraguchi,Takashi Ooi

Chem. Commun. 2017, 53, 6999-7002

DOI: 10.1039/C7CC02502E

Selected as a "Cover Picture"
64.

Unique Site-selectivity Control in Asymmetric Michael Addition of Azlactone to Alkenyl Dienyl Ketones Enabled by P-Spiro Chiral Iminophosphorane Catalysis

Ken Yoshioka, Kohei Yamada, Daisuke Uraguchi,Takashi Ooi

Chem. Commun. 2017, 53, 5495-5498

DOI: 10.1039/C7CC01715D

Themed Issue “Site-selective molecular transformations”

Selected as a "Cover Picture"
63. Acridinium Betaine as a Single-Electron-Transfer Catalyst: Design and Application to Dimerization of Oxindoles Daisuke Uraguchi, Masahiro Torii, Takashi Ooi ACS Catal. 2017, 7, 2765-2769 DOI: 10.1021/acscatal.7b00265
62. Complete diastereodivergence in asymmetric 1,6-addition reactions enabled by minimal modification of a chiral catalyst Daisuke Uraguchi, Ken Yoshioka, Takashi Ooi Nature Communications 2017, 8, 14793 DOI: 10.1038/ncomms14793 Highlighted in EurekAlert! Highlighted in Chem Europe Highlighted in Azom.com Highlighted in AlphaGalileo Highlighted in Phys.org プレスリリース (名古屋大学HP) 中日新聞(2017年4月4日)掲載
61.

[5.5]-P-Spirocyclic Chiral Triaminoiminophosphorane-Catalyzed Asymmetric Hydrophosphonylation of Aldehydes and Ynones

Daisuke Uraguchi, Takaki Ito, Yuto Kimura, Yumiko Nobori, Makoto Sato, Takashi Ooi

Bull. Chem. Soc. Jpn. 2017, 90, 546-555

DOI: 10.1246/bcsj.20170040

Highlighted as a "Selected Papers(SP)"
60.

In Situ Electrophilic Activation of Hydrogen Peroxide for Catalytic Asymmetric α-Hydroxylation of 3-Substituted Oxindoles

Kohsuke Ohmatsu, Yuichiro Ando, Takashi Ooi

Synlett 2017, 28, 1291-1294

DOI: 10.1055/s-0036-1558958

SYNLETT Cluster: Asymmetric Brønsted Base Catalysis

Selected as a " News article"

Selected as a " Front Cover"
59. Stereoselective Aza-Henry Reaction of 3-Nitro-Dihydro-2(1H)-Quinolones with N-BOC-Aldimines under the Catalysis of Chiral Ammonium Betaines Daisuke Uraguchi, Masahiro Torii, Kohsuke Kato, Takashi Ooi Heterocycles 2017, 94, 441-447 DOI: 10.3987/COM-16-13642
58. A Modular Strategy for the Direct Catalytic Asymmetric α-Amination of Carbonyl Compounds Kohsuke Ohmatsu, Yuichiro Ando, Tsubasa Nakashima, Takashi Ooi Chem 2016, 1, 802-810 DOI: 10.1016/j.chempr.2016.10.012 Highlighted in Chem-Station (化学者のつぶやき) Highlighted in Phys.Org Highlighted in Scienmag プレスリリース (名古屋大学HP) 中日新聞・日経産業新聞・日刊工業新聞 (2016年11月11日), 科学新聞（2016年11月25日）掲載
57. Origin of High Regio-, Diastereo-, and Enantioselectivities in 1,6-Addition of Azlactones to Dienyl N-Acylpyrroles: A Computational Study Yamanaka, Masahiro; Sakata, Ken; Yoshioka, Ken; Uraguchi, Daisuke; Ooi, Takashi J. Org. Chem. 2017, 82, 541-548 DOI: 10.1021/acs.joc.6b02572
56. Chiral Ammonium Betaine-Catalyzed Asymmetric Mannich-Type Reaction of Oxindoles Masahiro Torii, Kohsuke Kato, Daisuke Uraguchi, and Takashi Ooi Beilstein J. Org. Chem. 2016, 12, 2099-2103 DOI: 10.3762/bjoc.12.199 Thematic Series “Strategies in Asymmetric Catalysis”
55. Independence from the Sequence of Single-Electron Transfer of Photoredox Process in Redox-Neutral Asymmetric Bond-Forming Reaction Tomohito Kizu, Daisuke Uraguchi, and Takashi Ooi J. Org. Chem. 2016, 81, 6953-6958 DOI: 10.1021/acs.joc.6b00445 Special Issue on Photocatalysis
54.

Multiple Absolute Stereocontrol in Pd-Catalyzed [3+2] Cycloaddition of Oxazolidinones and Trisubstituted Alkenes Using Chiral Ammonium-Phosphine Hybrid Ligands

Naomichi Imagawa, Yuya Nagato, Kohsuke Ohmatsu, and Takashi Ooi

Bull. Chem. Soc. Jpn. 2016, 89, 649-656

DOI: 10.1246/bcsj.20160053

Selected as a "selected as BCSJ Award Article and Cover Picture"
53. Anion-Stoichiometry-Dependent Selectivity Enhancement in Ion-Paired Chiral Ligand-Palladium Complex Catalyzed Enantioselective Allylic Alkylation Kohsuke Ohmatsu, Yoshiyuki Hara, Yuya Kusano, Takashi Ooi Synlett 2016, 27, 1047-1050 DOI: 10.1055/s-0035-1561403 SYNLETT Cluster: Non-Covalent Interactions in Asymmetric Catalysis
52.

Palladium-Catalyzed Branch-Selective Decarboxylative Allylation Using Ion-Paired Ligands

Yoshiyuki Hara, Yuya Kusano, Kohsuke Ohmatsu, and Takashi Ooi

Chem. Lett. 2016, 45, 552-554

DOI: 10.1246/cl.160158

Selected as a "Editor's Choice"
51. Synergistic Catalysis of Ionic Brønsted Acid and Photosensitizer for a Redox Neutral Asymmetric α-Coupling of N-Arylaminomethanes with Aldimines Daisuke Uraguchi, Natsuko Kinoshita, Tomohito Kizu, and Takashi Ooi J. Am. Chem. Soc. 2015, 137, 13768-13771 DOI: 10.1021/jacs.5b09329 Highlighted in Synfacts 2016, 12, 0196. Highlighted in Organic Chemistry Portal.
50.

Enantioselective Reductive Multicomponent Coupling Reactions between Isatins and Aldehydes

Matthew A. Horwitz, Naoya Tanaka, Takuya Yokosaka, Daisuke Uraguchi, Jeffrey S. Johnson, and Takashi Ooi

Chem. Sci. 2015, 6, 6086-6090

DOI: 10.1039/C5SC02170G

Selected as a "Outside Back Cover"
49. Catalytic Asymmetric Cyanation of Alkylideneindolenines Generated from Sulfonylalkylindoles Kohsuke Ohmatsu, Yukino Furukawa, Daigo Nakaguro, and Takashi Ooi Chem. Lett. 2015, 44, 1350-1352 DOI: 10.1246/cl.150581
48. Highly E- and Enantioselective Michael Addition to Electron-deficient Internal Alkynes under the Catalysis of Chiral Iminophosphorane Daisuke Uraguchi, Kohei Yamada, Takashi Ooi Angew. Chem. Int. Ed. 2015, 54, 9954-9957 DOI: 10.1002/anie.201503928
47. Vinylogy in Nitronates: Utilization of α-Aryl Conjugated Nitroolefins as a Nucleophile for Highly Stereoselective Aza-Henry Reaction Keigo Oyaizu, Daisuke Uraguchi, Takashi Ooi Chem. Commun. 2015, 51, 4437-4439 DOI: 10.1039/C4CC10261D
46.

Palladium-Catalyzed Asymmetric [3 + 2] Cycloaddition of 5-Vinyloxazolidinones with Imines Using Chiral Ammonium-Phosphine Hybrid Ligand

Kohsuke Ohmatsu, Shinya Kawai, Naomichi Imagawa, Takashi Ooi

ACS Catal. 2014, 4, 4304-4306

DOI: 10.1021/cs501369z

Selected as a "Cover Picture"
45.

Chiral Ammonium Betaine-Catalyzed Highly Stereoselective Aza-Henry Reaction of α-Aryl Nitromethanes with Aromatic N-Boc Imines

Daisuke Uraguchi, Keigo Oyaizu, Haruhiro Noguchi, Takashi Ooi

Chem. Asian J. 2014, 10, 334-337

DOI: 10.1002/asia.201402943

Selected as a "Inside Cover"
44. Enantioselective Protonation of α-Hetero Carboxylic Acid-Derived Ketene Disilyl Acetals under Chiral Ionic Brønsted Acid Catalysis Daisuke Uraguchi, Tomohito Kizu, Yuki Ohira, Takashi Ooi Chem. Commun. 2014, 50,13489-13491 DOI: 10.1039/C4CC06081D
43. In-Situ Generation of Ion-Paired Chiral Ligands: Rapid Identification of Optimal Ligand for Palladium-Catalyzed Asymmetric Allylation Kohsuke Ohmatsu, Yoshiyuki Hara, Takashi Ooi Chem. Sci. 2014, 5, 3645-3650 DOI: 10.1039/C4SC01032A
42. Enantioselective formal α-allylation of nitroalkanes through a chiral iminophosphorane-catalyzed Michael reaction-Julia-Kocienski olefination sequence Daisuke Uraguchi, Shinji Nakamura, Hitoshi Sasaki, Yuki Konakade, Takashi Ooi Chem. Commun. 2014, 50, 3491-3493 DOI: 10.1039/C3CC49477B
41.

Practical Preparation of Chiral N-Sulfonyl Oxaziridines by Catalytic Asymmetric Payne Oxidation

Ryosuke Tsutsumi, Seonwoo Kim, Daisuke Uraguchi, Takashi Ooi

Synthesis (PSP article) 2014, 46, 871-878

DOI: 10.1055/s-0033-1340818

Highlighted in organic chemistry portal
40.

Ligand-controlled E/Z selectivity and enantioselectivity in palladium-catalyzed allylation of benzofuranones with 1,2-disubstituted allylic carbonates

Kohsuke Ohmatsu, Mitsunori Ito , Takashi Ooi

Chem. Commun. 2014, 50, 4554-4557

DOI: 10.1039/C3CC49338E

Highlighted in Synfacts 2014, 706.

Selected as a "Outside Back Cover"
39. Asymmetric Alkylation of α-Cyanosulfones Catalyzed by Chiral 1,2,3-Triazolium Salts Kohsuke Ohmatsu, Yusuke Hakamata, Ayano Goto, Takashi Ooi Heterocycles 2014, 88, 1661-1666 DOI: 10.3987/COM-13-S(S)121
38.

Catalytic asymmetric Payne oxidation under the catalysis of P-spiro chiral triaminoiminophosphorane: Application to the synthesis of N-sulfonyl oxaziridines

Daisuke Uraguchi, Ryosuke Tsutsumi, Takashi Ooi

Tetrahedron 2014, 70, 1691-1701

DOI: 10.1016/j.tet.2013.12.086

Highlighted as a cover figure
37. Asymmetric Substitution at the Tetrasubstituted Chiral Carbon: Catalytic Ring-Opening Alkylation of Racemic 2,2-Disubstituted Aziridines with 3-Substituted Oxindoles Kohsuke Ohmatsu, Yuichiro Ando , Takashi Ooi J. Am. Chem. Soc. 2013, 135, 18706-18709 DOI: 10.1021/ja411647x
36. Ligand-enabled multiple absolute stereocontrol in metal-catalysed cycloaddition for construction of contiguous all-carbon quaternary stereocenters Kohsuke Ohmatsu, Naomichi Imagawa, Takashi Ooi Nature Chem. 2014, 6, 47-51 DOI: 10.1038/nchem.1796 Highlighted in Synform 2014, A81-84. http://dx.doi.org/10.1055/s-0033-1339014 (Synstory) Highlighted in Synfacts 2014, 354. http://dx.doi.org/10.1055/s-0033-1341001 Highlighted in Chem-Station (化学者のつぶやき) プレスリリース (名古屋大学HP) 中日新聞・日経産業新聞 (2013年11月25日)掲載 CBCテレビ(2013年11月25日)
35. Carbene Transfer from Triazolylidene Gold Complexes as a Potent Strategy for Inducing High Catalytic Activity Daniel Canseco-Gonzalez, Ana Petronilho, Helge Mueller-Bunz, Kohsuke Ohmatsu, Takashi Ooi, Martin Albrecht J. Am. Chem. Soc. 2013, 135, 13193-13203 DOI: 10.1021/ja406999p
34. Catalytic Asymmetric Oxidation of N-Sulfonyl Imines with Hydrogen Peroxide－Trichloroacetonitrile System Daisuke Uraguchi, Ryosuke Tsutsumi, and Takashi Ooi J. Am. Chem. Soc. 2013, 135, 8161-8164 DOI: 10.1021/ja403491j Highlighted in Synfacts 2013, 1005.
33. Exploiting the Modularity of Ion-Paired Chiral Ligands for Palladium-Catalyzed Enantioselective Allylation of Benzofuran-2(3H)-ones Kohsuke Ohmatsu, Mitsunori Ito, Tomoatsu Kunieda, and Takashi Ooi J. Am. Chem. Soc. 2013, 135, 590－593 DOI: 10.1021/ja312125a Highlighted in Synfacts 2013, 407.
32. Highly Stereoselective Michael Addition of Azlactones to Electron-Deficient Triple Bonds under P-Spiro Chiral Iminophosphorane Catalysis: Importance of Protonation Pathway Uraguchi, Daisuke; Ueki, Yusuke; Sugiyama, Atsushi; Ooi, Takashi Chem. Sci. 2013, 4, 1308-1311 DOI: 10.1039/C2SC22027J
31. Highly Regio-, Diastereo-, and Enantioselective 1,6- and 1,8-Additions of Azlactones to Di- and Trienyl N-Acylpyrroles Uraguchi, Daisuke; Yoshioka, Ken; Ueki, Yusuke; Ooi, Takashi J. Am. Chem. Soc. 2012, 134, 19370-19373. DOI: 10.1021/ja311719f Highlighted in JACS Spotlights Highlighted in Synfacts 2013, 217. http://dx.doi.org/10.1055/s-0032-1318035
30.

Chiral Ionic Brønsted Acid-Achiral Brønsted Base Synergistic Catalysis for Asymmetric Sulfa-Michael Addition to Nitroolefins

Uraguchi, Daisuke; Kinoshita, Natsuko; Nakashima, Daisuke; Ooi, Takashi

Chem. Sci. 2012, 3, 3161-3164.

DOI: 10.1039/C2SC20698F

Selected as a "Outside Back Cover"
29. Catalytic Asymmetric Ring Openings of Meso and Terminal Aziridines with Halides Mediated by Chiral 1,2,3-Triazolium Silicates Ohmatsu, Kohsuke; Hamajima, Yuta; Ooi, Takashi J. Am. Chem. Soc. 2012, 134, 8794-8797. DOI: 10.1021/ja3028668 Highlighted in Synfacts 2012, 892. http://dx.doi.org/10.1055/s-0032-1316631 Highlighted in Synfacts 2012, 911. http://dx.doi.org/10.1055/s-0032-1316697
28.

Catalytic Asymmetric Mannich-Type Reactions of α-Cyano α-Sulfonyl Carbanions

Ohmatsu, Kohsuke; Goto, Ayano; Ooi, Takashi

Chem. Commun. 2012, 48, 7913-7915.

DOI: 10.1039/C2CC32398B

Selected as a "Cover Picture"
27. Nitroolefins as a Nucleophilic Component for Highly Stereoselective Aza-Henry Reaction under the Catalysis of Chiral Ammonium Betaines Uraguchi, Daisuke; Oyaizu, Keigo; Ooi, Takashi Chem. Eur. J. 2012, 18, 8306-8309. DOI: 10.1002/chem.201201259
26. Ionic Nucleophilic Catalysis of Chiral Ammonium Betaines for Highly Stereoselective Aldol Reaction from Oxindole-Derived Vinylic Carbonates Uraguchi, Daisuke; Koshimoto, Kyohei; Ooi, Takashi J. Am. Chem. Soc. 2012, 134, 6972-6975. DOI: 10.1021/ja3022939 Highlighted in Synfacts 2012, 670. http://dx.doi.org/10.1055/s-0031-1291036
25. Ion-paired chiral ligands for asymmetric palladium catalysis Ohmatsu, Kohsuke; Ito, Mitsunori; Kunieda, Tomoatsu; Ooi, Takashi Nat. Chem. 2012, 4, 473-477. DOI:10.1038/nchem.1311 Highlighted in Nature Chemistry (News and Views) Highlighted in Synfacts 2012, 876. http://dx.doi.org/10.1055/s-0032-1316660 Highlighted in Synform 2012, A113-A114. http://dx.doi.org/10.1055/s-0032-1316780 (Synstory) プレスリリース (名古屋大学HP) 中日新聞 (2012年4月2日朝刊)掲載 NHKおはよう東海(2012年4月2日)
24. Base-Catalyzed Direct Aldolization of α-Alkyl-α-Hydroxy Trialkyl Phosphonoacetates Corbett, Michael; Uraguchi, Daisuke; Ooi, Takashi; Johnson, Jeffrey Angew. Chem. Int. Ed. 2012, 51, 4685-4689. DOI: 10.1002/anie.201200559
23. Highly Stereoselective Catalytic Conjugate Addition of Acyl Anion Equivalent to Nitroolefins Uraguchi, Daisuke; Ueki, Yusuke; Ooi, Takashi Chem. Sci. 2012, 3, 842-845. DOI: 10.1039/C1SC00678A
22. Enantioselective Aza-Michael Addition to Conjugated Nitroenynes Catalyzed by Chiral Arylaminophosphonium Barfates Uraguchi, Daisuke; Kinoshita, Natsuko; Kizu, Tomohito; Ooi, Takashi Synlett. 2011, 1265-1267. https://www.thieme-connect.com/ejournals/html/synlett/doi/10.1055/s-0030-1260541 SYNLETT Cluster: Brønsted Acid Catalysis
21. Precise Control of Spontaneous Molecular Assembly of Chiral Tetraaminophosphonium Aryloxide-Arylhydroxide(s) in Solution Uraguchi, Daisuke; Ueki, Yusuke; Ooi, Takashi Angew. Chem. Int. Ed. 2011, 50, 3681-3683. DOI: 10.1002/anie.201007752 Selected as "Hot Paper"
20. Chiral 1,2,3-Triazoliums as New Cationic Organic Catalysts with Anion-Recognition Ability: Application to Asymmetric Alkylation of Oxindoles Ohmatsu, Kohsuke, Kiyokawa, Mari, Ooi, Takashi J. Am. Chem. Soc. 2011, 133, 1307-1309. DOI: 10.1021/ja1102844 Highlighted in Synfacts 2011, 324. http://dx.doi.org/10.1055/s-0030-1259452
19. Catalytic Asymmetric Protonation of α-Amino Acid-Derived Ketene Disilyl Acetals Using P-Spiro Diaminodioxaphosphonium Barfates as Chiral Proton Uraguchi, Daisuke; Kinoshita, Natsuko; Ooi, Takashi J. Am. Chem. Soc. 2010, 132, 12240-12242. DOI: 10.1021/ja105945z Highlighted in Synfacts 2010, 1300. http://dx.doi.org/10.1055/s-0030-1258790
18. Catalytic Asymmetric Direct Henry Reaction of Ynals: Short Syntheses of (2S,3R)-(+)-Xestoaminol C and (-)-Codonopsinines Uraguchi, Daisuke; Nakamura, Shinji; Ooi, Takashi Angew. Chem. Int. Ed. 2010, 49, 7562-7565. DOI: 10.1002/anie.201004072 Highlighted in Synfacts 2010, 1309. http://dx.doi.org/10.1055/s-0030-1258782
17. Chiral Ammonium Betaines as an Ionic Nucleophilic Catalyst Uraguchi, Daisuke; Koshimoto, Kyohei; Miyake, Shuhei; Ooi, Takashi Angew. Chem. Int. Ed. 2010, 49, 5567-5569. DOI: 10.1002/anie.201002315 Highlighted in Synfacts 2010, 1075. http://dx.doi.org/10.1055/s-0030-1257971
16. Catalytic Asymmetric Hydrophosphonylation of Ynones Uraguchi, Daisuke; Ito, Takaki; Nakamura, Shinji; Ooi, Takashi Chem. Sci. 2010, 1, 488-490. DOI: 10.1039/c0sc00268b Highlighted in Synfacts 2011, 50. http://dx.doi.org/10.1055/s-0030-1259171
15. Performance of C1-symmetric chiral ammonium betaines as a catalyst for the enantioselective Mannich-type reaction of α-nitrocarboxylates Uraguchi, Daisuke; Koshimoto, Kyohei; Sanada, Chisato; Ooi, Takashi Tetrahedron: Asymmetry. 2010, 21, 1189-1190. http://dx.doi.org/10.1016/j.tetasy.2010.04.006
14. Flexible Synthesis, Structural Determination, and Synthetic Application of a New C1-Symmetric Chiral Ammonium Betaine Uraguchi, Daisuke; Koshimoto, Kyohei; Ooi, Takashi Chem. Commun. 2010, 46, 300-302. http://www.rsc.org/Publishing/Journals/CC/article.asp?doi=b916627k Selected as "Hot Article" Highlighted in Synfacts 2010, 0232. http://dx.doi.org/10.1055/s-0029-1219139
13. Diastereo- and Enantioselective Direct Henry Reaction of Pyruvates Mediated by Chiral P-Spiro Tetraaminophosphonium salts Uraguchi, Daisuke; Ito, Takaki; Nakamura, Shinji; Sakaki, Sawako; Ooi, Takashi Chem. Lett. 2009, 38, 1052. http://www.jstage.jst.go.jp/article/cl/38/11/38_1052/_article
12. Chiral Organic Ion Pair Catalysts Assembled Through a Hydrogen-Bonding Network Uraguchi, Daisuke; Ueki, Yusuke; Ooi, Takashi Science. 2009, 326, 120-123. http://www.sciencemag.org/cgi/content/abstract/326/5949/120 Highlighted in C & EN 2009, 87, 25-26. [Science & Technology Concentrates (August 31)] プレスリリース (名古屋大学HP) 読売新聞、日刊工業新聞 (8月28日朝刊)掲載 Highlighted in Synfacts 2009, 1408. http://dx.doi.org/10.1055/s-0029-1218214 Highlighted in ACIE DOI: 10.1002/anie.200906392
11. Al Lewis acid-catalyzed regiodivergent 1,2-rearrangement of α-siloxy aldehydes: scope and mechanism Ohmatsu, Kohsuke; Tanaka, Takayuki; Ooi, Takashi; Maruoka, Keiji Tetrahedron 2009, 65, 7516-7522. http://dx.doi.org/10.1016/j.tet.2009.06.126
10. Chiral Arylaminophosphonium Barfates as a New Class of Charged Brønsted Acid for the Enantioselective Activation of Nonionic Lewis Bases Uraguchi, Daisuke; Nakashima, Daisuke; Ooi, Takashi J. Am. Chem. Soc. 2009, 131, 7242-7243. http://pubs.acs.org/doi/abs/10.1021/ja903271t Highlighted in Synfacts 2009, 562. http://dx.doi.org/10.1055/s-0029-1217582
9. Generation of Chiral Phosphonium Dialkyl Phosphite as a Highly Reactive P-Nucleophile: Application to Asymmetric Hydrophosphonylation of Aldehydes Uraguchi, Daisuke; Ito, Takaki; Ooi, Takashi J. Am. Chem. Soc. 2009, 131, 3836-3837. http://pubs.acs.org/doi/abs/10.1021/ja810043d Correction J. Am. Chem. Soc. 2017, 139,3299?3299. http://pubs.acs.org/doi/abs/10.1021/jacs.7b01263 Highlighted in Synfacts 2009, 562. http://dx.doi.org/10.1055/s-0029-1216583 Highlighted in Synfacts 2009, 645. http://dx.doi.org/10.1055/s-0029-1216717
8. Asymmetric Synthesis of α,α-Disubstituted-α-Amino Acids via Enantioselective Alkylation of Azlactones under Biphasic Conditions Using P-Spiro Chiral Tetraaminophosphonium Salts as a Phase-Transfer Catalyst Uraguchi, Daisuke; Asai, Yoshihiro; Seto, Yuki; Ooi, Takashi Synlett 2009, 658-660. http://www.thieme-connect.com/ejournals/abstract/synlett/doi/10.1055/s-0028-1087812 SYNLETT Cluster: Phase Transfer Catalyst for Asymmetric Synthesis
7.

Site-directed Asymmetric Quaternization of a Peptide Backbone at a C-Terminal Azlactone

Uraguchi, Daisuke; Asai, Yoshihiro; Ooi, Takashi

Angew. Chem. Int. Ed. 2009, 48, 733-737.

http://www.thieme-connect.com/ejournals/abstract/synlett/doi/10.1055/s-0028-1087812

Selected as a "inside cover picture"

Highlighted in Synfacts 2009, 205. http://dx.doi.org/10.1055/s-0028-1087586
6. Chiral Tetraaminophosphonium Carboxylate-Catalyzed Direct Mannich-Type Reaction Uraguchi, Daisuke; Ueki, Yusuke; Ooi, Takashi J. Am. Chem. Soc. 2008, 130, 14088-14089. http://pubs.acs.org/cgi-bin/abstract.cgi/jacsat/asap/abs/ja806311e.html Highlighted in Synfacts 2008, 1327. http://dx.doi.org/10.1055/s-0028-1083579
5. Chiral Ammonium Betaines: A Bifunctional Organic Base Catalyst for Asymmetric Mannich-type Reaction of α-Nitrocarboxylates Uraguchi, Daisuke; Koshimoto, Kyohei; Ooi, Takashi J. Am. Chem. Soc. 2008, 130, 10878-10879. http://pubs.acs.org/cgi-bin/abstract.cgi/jacsat/asap/abs/ja8041004.html Highlighted in Synfacts 2008, 1105. http://dx.doi.org/10.1055/s-2008-1078149 (Synfact of the month)
4. Synthesis of Chiral Tetraaminophosphonium Chlorides from N-BOC α-Amino Acid Esters Uraguchi, Daisuke; Sakaki, Sawako; Ueki, Yusuke; Ito, Takaki; Ooi, Takashi Heterocycles 2008, 76, 1081-1085. http://www.heterocycles.jp/library/abstract.php?article=3158
3. Chiral Tetraaminophosphonium Salt-Mediated Asymmetric Direct Henry Reaction Uraguchi, Daisuke; Sakaki, Sawako; Ooi, Takashi J. Am. Chem. Soc. 2007, 129, 12392-12393. http://pubs.acs.org/cgi-bin/abstract.cgi/jacsat/2007/129/i41/abs/ja075152+.html Highlighted in Synfacts 2007, 1309. http://dx.doi.org/10.1055/s-2007-991331 (Synfact of the month) Highlighted in Synform 2007, A7-A8. http://dx.doi.org/10.1055/s-2007-1000843 (Synstory)
2. Advantage of in situ generation of N-arylsulfonyl imines from α-amide sulfones in the phase-transfer-catalyzed asymmetric Strecker reaction Ooi, Takashi; Uematsu, Yukitaka; Fujimoto, Jun; Fukumoto, Kazuhiro; Maruoka, Keiji Tetrahedron Letters 2007, 48, 1337-1340. http://dx.doi.org/10.1016/j.tetlet.2006.12.122
1. Asymmetric Strecker Reaction of Aldimines Using Aqueous Potassium Cyanide by Phase-Transfer Catalysis of Chiral Quaternary Ammonium Salts with a Tetranaphthyl Backbone. Ooi, Takashi; Uematsu, Yukitaka; Maruoka, Keiji J. Am. Chem. Soc 2006, 128, 2548-2549. http://dx.doi.org/10.1021/ja058066n

総説等 : Reviews

12.

Catalytic acceptorless dehydrogenative coupling mediated by photoinduced hydrogen-atom transfer

Kohsuke Ohmatsu, Takashi Ooi

Nature Synth. 2023, xx, xxxx-xxxx.

DOI: 10.1038/s44160-022-00195-1
11. Catalysis of chiral iminophosphorane for simultaneous control of multiple selectivity: experimental and theoretical investigation 浦口大輔, 大井貴史 有機合成化学協会誌 2021, 79, 406-416. https://doi.org/10.5059/yukigoseikyokaishi.79.406
10. Cationic Organic Catalysts or Ligands in Concert with Metal Kohsuke Ohmatsu, Takashi Ooi Topics in Current Chemistry 2019, 377, 31. https://link.springer.com/article/10.1007/s41061-019-0256-1
9. Chemistry of Ammonium Betaines: Application to Ion-Pair Catalysis for Selective Organic Transformations 浦口大輔, 大井貴史 有機合成化学協会誌 2018, 76, 1144-1153. https://doi.org/10.5059/yukigoseikyokaishi.76.1144
8. Design of supramolecular chiral ligands for asymmetric metal catalysis Kohsuke Ohmatsu, Takashi Ooi Tetrahedron Letters 2015, 56, 2043-2048. http://dx.doi.org/10.1016/j.tetlet.2015.02.096
7. Development of Ion-Paired Chiral Ligands for Asymmetric Transition-Metal Catalysis 大松亨介, 大井貴史 有機合成化学協会誌 2015, 73, 140-150. http://doi.org/10.5059/yukigoseikyokaishi.73.140
6. Development of P-Spiro Chiral Aminophosphonium Salts as a New Class of Versatile Organic Molecular Catalyst 浦口大輔, 大井貴史 有機合成化学協会誌 2010, 68, 1185-1194. http://www.jstage.jst.go.jp/article/yukigoseikyokaishi/68/11/1185/_pdf/-char/ja/
5. 「水素結合供与型キラルホスホニウム/有機アニオンが示す新たなイオン「対」触媒作用」 上木佑介, 浦口大輔, 大井貴史 触媒 2010, 52, 509-514. http://www.shokubai.org/jnl/tmpPdf/1295275473a.pdf
4. 「P-スピロ型テトラアミノホスホニウム塩の創製と有機分子触媒としての機能発現」 浦口大輔 触媒 2008, 50, 683-687. PermaLink
3. Development and Applications of C₂-Symmetric, Chiral, Phase-Transfer Catalysts Ooi, Takashi; Maruoka, Keiji Aldrichimia Acta 2007, 40, 77-86. http://www.sigmaaldrich.com/aldrich/acta/al_acta_40_03.pdf
2. Design of Chiral Organocatalysts for Practical Asymmetric Synthesis of Amino Acid Derivatives Maruoka, Keiji; Ooi, Takashi; Kano, Taichi Chem. Commun. 2007, 1487-1495. DOI: 10.1039/b613049f
1. Recent Advances in Asymmetric Phase-Transfer Catalysis Ooi, Takashi; Maruoka, Keiji Chem. Commun. 2007, 46, 4222-4266. DOI: 10.1002/anie.200601737

解説・紀要等

10. 「人工ストリゴラクトンの設計」 土屋雄一朗, 浦口大輔, 大井貴史 植物の生長調節 2019, 54(1), 49-53. https://doi.org/10.18978/jscrp.54.1_49
9. 「有機イオン対の触媒化学：構造に由来する機能発現」 浦口大輔, 大松亨介, 大井貴史 ケミカルタイムズ 2018, (2), 20-26. https://www.kanto.co.jp/dcms_media/other/CT_248_all.pdf
8. 「有機分子触媒の化学－「輪」をもって尊しとなす－」 浦口大輔, 大井貴史 現代化学 2017, 558(9), 52-56.
7. α-アミノカルボニル化合物の効率的不斉合成 中島翼，大松亨介, 大井貴史 PHARMSTAGE 2017, 17, 61-67.
6. 「[5.5]-P-スピロ型キラルテトラアミノホスホニウム塩を用いる触媒的分子変換」 浦口大輔, 大井貴史 Wako Organic Square 2017, 59(3), 2-5. http://www.wako-chem.co.jp/siyaku/journal/org/pdf/org59.pdf
5. 「Lectureship Award MBLA 2014受賞講演ツアーを終えて」 浦口大輔 有機合成化学協会誌 2015, 73, 653-662. http://doi.org/10.5059/yukigoseikyokaishi.73.653
4. 「忘れられた反応剤Davis’オキサジリジン」 浦口大輔, 堤亮祐, 大井貴史 月刊「化学」 2013, 68, 66-67.
3. 「D₂対称型光学活性テトラアミノホスホニウム塩の創製と相間移動触媒反応への応用」 浦口大輔, 大井貴史 月刊ファインケミカル 2010, 39, 42-48.
2. 「光学活性な炭素の三角形を作る―Corey-Chaykovsky反応と親電子剤活性化法の組み合わせ」 浦口大輔, 大井貴史 化学 2008, 63, 66-67.
1. 「二相系でのイミンの系内発生を活かした触媒的不斉合成」 大井貴史 Organometallic News 2008, 40-43

著書等 : Books

14. “Organic Molecular Catalysts in Radical Chemistry: Challenges Toward Selective Transformations” Daisuke Uraguchi, Kohsuke Ohmatsu, Takashi Ooi “Molecular Technology: Synthesis Innovation, Volume 4” H. Yamamoto and T. Kato Eds. Wiley-VCH; 163-197 (2019)
13. 「多機能型キラルオニウム塩の設計に基づく高選択的分子変換」 大松亨介, 浦口大輔, 大井貴史 “有機分子触媒の開発と工業利用” シーエムシー出版; xxx-xxx (2018)
12. 「イオン対を中心とした不斉塩基触媒」 浦口大輔, 大井貴史 “CSJカレントレビュー「有機分子触媒の化学」” 日本化学会; 109-117 (2016)
11. “Site-Selective Conjugate Addition through Catalytic Generation of Ion-Pairing Intermediates” Daisuke Uraguchi, Takashi Ooi “Topics in Current Chemistry: Site Selective Catalysis” T. Kawabata Ed. Springer; 55-84 (2016)
10. 「イオン性キラル触媒～新しい分子設計へのこだわり～」 大松亨介, 大井貴史 “CSJカレントレビュー「キラル化学：その起源から最新のキラル材料研究まで」” 八島栄治日本化学会; (2013)
9. “Axially Chiral C₂-Symmetric Catalysts” Daisuke Uraguchi, Kohsuke Ohmatsu, Takashi Ooi “Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications” P. I. Dalko Eds. Wiley-VCH; 161-193 (2013)
8. “Asymmetric phase-transfer catalysis” Kohsuke Ohmatsu, Daisuke Uraguchi, Takashi Ooi “Stereoselective Synthesis of Drugs and Natural Products” V. Andrushko, N. Andrushko Eds. Wiley-VCH; 119-144 (2013)
7. "6.1 C-C Bond Formation: Alkylation" Uraguchi, Daisuke; Ooi, Takashi "COMPREHENSIVE CHIRALITY" Elsevier Science; 1-36 (2012)
6. "Hydrogen-Bonding Catalysts Other than Ureas and Thioureas" Uraguchi, Daisuke; Ooi, Takashi "Science of Synthesis: Asymmetric Organicatalysis 2" Thieme; 413-435 (2012)
5. "Development of phase-transfer-catalyzed asymmetric Strecker reaction based on the molecular design of chiral quaternary ammonium salts" Ooi, Takashi "ACS Symposium Series (2009), 1009(Asymmetric Synthesis and Application of .alpha.-Amino Acids)" ACS Publications; 177-189 (2009)
4. “Chiral quaternary ammonium fluorides for asymmetric synthesis” Shirakawa, Seiji; Ooi, Takashi; Maruoka, Keiji “Asymmetric Phase Transfer Catalysis” K. Maruoka Eds. Wiley-VCH; 189-206 (2008)
3. “Cinchona-derived chiral phase-transfer catalysts for amino acid synthesis” T. Ooi “Asymmetric Phase Transfer Catalysis” K. Maruoka Eds. Wiley-VCH; 9-33 (2008)
2. “Chiral Carbonyl Lewis Acid Complexes in Asymmetric Syntheses” K. Maruoka, T. Ooi “Asymmetric Synthesis - The Essentials” M. Christmann, S. Bräse Eds. VCH; 121-125 (2007)
1. “Ammonium Ions as Chiral Templates” T. Ooi, K. Maruoka “Enantioselective Organocatalysis: Reactions and Experimental Procedures” P. I. Dalko Ed. Wiley; 121-150 (2007)