2023-2021
★は更新した部分です。
2023
★129.Tetsuhiro Nemoto:
Advances in the synthesis of dragmacidin E
Tetrahedron Letters 125, 154626 (2023).
Tetsuhiro Nemoto:
Development of Transition-Metal-Catalyzed Dearomatization Reactions
Chem. Pharm. Bull. 71, 624 (2023).
127.
Yu Matsuda, Masaya Nakajima, and Tetsuhiro Nemoto:
Acridine PNP-Pincer Ligands Enabling Transition Metal-Catalyzed Photoreactions
ACS Catalysis, 13, 10224 (2023) .
126.
Momoka Chiba, Mai Yanagawa, Yurika Oyama, Shingo Harada, Tetsuhiro Nemoto, Akira Matsuura, and Eisuke Itakura:
A novel autophagy inhibitor, bTBT, disturbs autophagosome formation
Autophagy Reports 13 2194620 (2023).
125.
Kotaro Ikeda, Shingo Harada, Yoshinori Hashimoto, Haruka Homma, Masato Kono, Nadine Zumbragel, Harald Groger, and Tetsuhiro Nemoto:
Enantioselective Formal Synthesis of (ー)-Catharanthine via Enzyme-Catalyzed Desymmetrization of meso-Azabicyclo[2.2.2]octane
Synlett., (2023) in press.
A Special Synlett Cluster for the SICC-11 meeting
124.
Dongil Choi, Noa Takahashi, Haruka Maruoka, Shingo Harada, Alina Nastke, Harald Groger, and Tetsuhiro Nemoto:
Synthetic Study of Dragmacidin E: Enantioselective Construction of the Seven-Membered Ring-Fused Indole Skeleton with Contiguous Stereocenters.
J. Org. Chem., 88, 7674 (2023).
Special Issue "Mordern Enantioselective Catalysis in Organic Chemistry"
123.
Tsukasa Furuya, Kotaro Ikeda, Shingo Harada, Tetsuhiro Nemoto:
Theoretical Investigation of Chemoselectivity between C-H Insertion and Amide Insertion in Intramolecular Rhodium-Carbene Reactions.
Chem. Pharm. Bull., 2, 107 (2023).
Current Topics - Transition Metal Catalysis Research in Pharmaceutical Organic Chemistry
122.
Tsubasa Ito, Shingo Harada, Haruka Homma, Ayaka Okabe, and Tetsuhiro Nemoto:
Mechanistic Investigation on Dearomative Spirocyclization of Arenes with α-Diazoamide under Boron Catalysis
ACS Catalysis, 13, 147 (2023).
千葉大プレスリリース
Chem-Stationスポットライトリサーチ
2022
121.
Yoshinori Hashimoto, Shingo Harada, Ryosuke Kato, Kotaro Ikeda, Jannis Nonnhoff, Harald Groger, and Tetsuhiro Nemoto:
Merging Chemo- and Biocatalysis to Facilitate Syntheses of Complex Natural Products: Enantioselective Construction of N-Bridged [3.3.1] Ring System in Indole Terpenoids
ACS Catalysis, 12, 14990 (2022).
千葉大プレスリリース
Chem-Stationスポットライトリサーチ
120.
Takato Inoue, Kazuaki Matsuda, Keisuke Matsusaka, Masaya Nakajima,Yukari Takeno, Toko Miyazaki, Takahiko Shintaku, Natsumi Yoda, Takahiko Saito, Eriko Ikeda, Yasunobu Mano, Kenichi Shinohara, Bahityar Rahmutulla, Masaki Fukuyo, Kazuko Kita, Tetsuhiro Nemoto, Atsushi Kaneda:
Anti-proliferating and apoptosis-inducing activity of chemical compound FTI-6D in association with p53 in human cancer cell lines
Chem. Biol. Intaract., 369, 110257 (2022).
119.
Masaya Nakajima, Toshiyasu Yamauchi, Yusuke Adachi, and Tetsuhiro Nemoto:
Computation-Guided Total Synthesis of Vitisinol G
Chem. Pharm. Bull., 70, 735 (2022).
118.
Takahito Kuribara, Masaya Nakajima & Tetsuhiro Nemoto:
A visible-light activated secondary phosphine oxide ligand enabling Pd-catalyzed radical cross-couplings
Nature Communications, 13, 4052 (2022).
千葉大プレスリリース
Chem-Stationスポットライトリサーチ
117.
Tsubasa Ito, Jun Ueda, Shingo Harada, Tetsuhiro Nemoto:
Development of Selective Molecular Transformations Based on Unique Chemical Properties of Silver Catalyst: A Theoretical Analysis and Experimental Verification
J. Synth. Org. Chem., Jpn, 80, 440 (2022).
116.
Masaya Nakajima, Sho Nagasawa, Koki Matsumoto, Yu Matsuda, Tetsuhiro Nemoto:
Synthesis of Visible-Light—Activated Hypervalent Iodine and Photo-oxidation under Visible Light Irradiation via a Direct S0→Tn Transition
Chem. Pharm. Bull., 70, 235 (2022).
115.
Masaya Nakajima, Yusuke Adachi & Tetsuhiro Nemoto:
Computation-guided asymmetric total syntheses of resveratrol dimers
Nature Communications, 13, 152 (2022).
千葉大プレスリリース
114.
Tomohiro Yazawa, Masaya Nakajima, and Tetsuhiro Nemoto:
ABNORMAL STRECKER REACTION OF 3-FORMYLINDOLE AND ANILINE
HETEROCYCLES, 13, 532 (2022).
【HETEROCYCLES Special Issue Vol. 105 in honor of Professor Somsak Ruchirawat on 80th Birthday】
2021
113.
Masaya Nakajima, and Tetsuhiro Nemoto:
Machine learning enabling prediction of the bond dissociation enthalpy of hypervalent iodine from SMILES
Sci. Rep., 11, 20207 (2021).
千葉大プレスリリース
112.
Takahito Kuribara, Masaya Nakajima, and Tetsuhiro Nemoto:
Mechanistic Studies of the Pd- and Pt-Catalyzed Selective Cyclization of Propargyl/Allenyl Complexes
J. Org. Chem., 86, 9670 (2021).
111.
Mai Yanagawa, Shingo Harada, Shumpei Hirose, Tetsuhiro Nemoto:
Rapid Synthesis of Functionalized Hydrocarbazolones via Indole C2-H Activation Using Enone Functionality as a Directing Group/Electrophilic Species
Adv. Synth. Catal., 363, 2189 (2021).
110.
Jun Ueda, Shingo Harada, Mayu Kobayashi, Mai Yanagawa, Tetsuhiro Nemoto:
Maleic Acid/Thiourea‐Catalyzed Dearomative ipso‐Friedel-Crafts Reaction of Indoles to Produce Functionalized Spiroindolenines
Eur. J. Org. Chem., 3999 (2021).
109.
Tsubasa Ito, Hiroki Takenaka, Haruka Homma, Shingo Harada, Tetsuhiro Nemoto:
Stereoselective construction of fused cyclopropane from ynamide and its application to synthesis of small drug candidate molecules
Tetrahedron Lett., 70, 152985(2021).
108.
Mitsuru Ikeda, Hiroki Nakayama, Ayaka Kanda, Shingo Harada, Tetsuhiro Nemoto:
Synthetic Studies on Didymeline Using Spirocyclization of Phenols with Diazo Functionality
HETEROCYCLES, 103, 687 (2021).
【Dedicated with respect to Professor Yasuyuki Kita on his 77th birthday】
107.
Zhaotong Wang, Takamasa Mizoguchi, Takahito Kuribara, Masaya Nakajima, Mayuu Iwata, Yuka Sakamoto, Hiroyuki Nakamura, Toshihiko Murayama, Tetsuhiro Nemoto, Motoyuki Itoh
Py3-FITC:a new fluorescent probe for live cell imaging of collagen-rich tissues and ionocytes
Open Biol., 11, 200241 (2021).
106.
Tsubasa Ito, Shingo Harada, Haruka Homma, Hiroki Takenaka, Shumpei Hirose, and Tetsuhiro Nemoto:
Asymmetric Intramolecular Dearomatization of Nonactivated Arenes with Ynamides for Rapid Assembly of Fuced Ring System under Silver Catalysis
J. Am. Chem. Soc., 143, 604 (2021).
千葉大プレスリリース
listed as one of the most cited publications from 2020-2021 in JACS
