A mild method for synthesizing carboxylic acids by oxidation of aldoximes using hypervalent iodine reagents

Akira Nakamura, Hodaka Kanou, Junki Tanaka, Akira Imamiya, Tomohiro Maegawa and Yasuyoshi Miki

Org. Biomol. Chem., 2018, 16, 541
DOI: 10.1039/C7OB02858J

Selective synthesis of 3-formylbenzofuran and 3-acylbenzofuran using a chalcone rearrangement strategy

Akira Nakamura, Akira Imamiya, Yuichiro Ikegami, Fei Rao, Harumi Yuguchi, Yasuyoshi Miki and Tomohiro Maegawa

RSC Adv., 2022, 12, 30426
DOI: 10.1039/D2RA06080A

A diversity oriented synthesis of natural product inspired molecular libraries

Jyoti Chauhan, Tania Luthra, Rambabu Gundla, Antonio Ferraro, Ulrike Holzgrabe and Subhabrata Sen

Org. Biomol. Chem., 2017, 15, 9108
DOI: 10.1039/C7OB02230A

A concise synthesis of thioauronesviaNBS-induced cyclization of MOM-protected 2′-mercaptochalcones

Akira Nakamura, Fei Rao, Kazuchika Ukiya, Riko Matsunaga, Shin-ichiro Ohira and Tomohiro Maegawa

Org. Biomol. Chem., 2023, 21, 1134
DOI: 10.1039/D2OB01995G

Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated oxysulfonyloxylation of alkynes with sulfonic acids

Yang Zhang, Hua Tan and Weibing Liu

RSC Adv., 2017, 7, 54017
DOI: 10.1039/C7RA11875A

The green chemistry of chalcones: Valuable sources of privileged core structures for drug discovery

Ludovica Marotta, Sara Rossi, Roberta Ibba, Simone Brogi, Vincenzo Calderone, Stefania Butini, Giuseppe Campiani and Sandra Gemma

Front. Chem., 2022, 10
DOI: 10.3389/fchem.2022.988376

Regioselective Synthesis of 3,4-Disubstituted Isoxazoles by Using a Chalcone-Rearrangement Strategy

Akira Nakamura, Tohko Kine, Haruna Uenishi, Yuri Maki, Yasuhito Kase, Mayo Takagi and Tomohiro Maegawa

Synlett, 2023, 34, 1253
DOI: 10.1055/a-2028-9454

The Reaction of Ketoximes with Hypervalent Iodine Reagents: Beckmann Rearrangement and Hydrolysis to Ketones

Tomohiro Maegawa, Ryohei Oishi, Ayumi Maekawa, Kazutoshi Segi, Hiromi Hamamoto, Akira Nakamura and Yasuyoshi Miki

Synthesis, 2022, 54, 4095
DOI: 10.1055/a-1835-2188

Organofluorine chemistry: promising growth areas and challenges

Larisa V. Politanskaya, Galina A. Selivanova, Elena V. Panteleeva, Evgeny V. Tretyakov, Vyacheslav E. Platonov, Pavel V. Nikul’shin, Andrey S. Vinogradov, Yaroslav V. Zonov, Victor M. Karpov, Tatyana V. Mezhenkova, Aleksander V. Vasilyev, Andrei B. Koldobskii, Olga S. Shilova, Sofia M. Morozova, Yanina V. Burgart, Evgeny V. Shchegolkov, Victor I. Saloutin, Vladimir B. Sokolov, Aleksey Yu. Aksinenko, Valentine G. Nenajdenko, Mikhail Yu. Moskalik, Vera V. Astakhova, Bagrat A. Shainyan, Andrey A. Tabolin, Sema L. Ioffe, Vasiliy M. Muzalevskiy, Elizaveta S. Balenkova, Alexey V. Shastin, Andrey A. Tyutyunov, Vladimir E. Boiko, Sergei M. Igumnov, Alexander D. Dilman, Nicolay Yu. Adonin, Vadim V. Bardin, Salekh M. Masoud, Daria V. Vorobyeva, Sergey N. Osipov, Emiliya V. Nosova, Galina N. Lipunova, Valery N. Charushin, Darya O. Prima, Arkady G. Makarov, Andrey V. Zibarev, Boris A. Trofimov, Lyubov N. Sobenina, Kseniya V. Belyaeva, Vyacheslav Ya. Sosnovskikh, Dmitrii L. Obydennov and Sergey A. Usachev

Russ. Chem. Rev., 2019, 88, 425
DOI: 10.1070/RCR4871

Direct Synthesis of Chalcones from Anilides with Phenyl Vinyl Ketones by Oxidative Coupling Through C–H Bond Activation

Tomohiro Maegawa, Ryota Mizui, Miki Urasaki, Kazuma Fujimura, Akira Nakamura and Yasuyoshi Miki

ACS Omega, 2018, 3, 5375
DOI: 10.1021/acsomega.8b00594

Development of Synthetic Methods for Heterocyclic Compounds Using the Oxidative Rearrangement of Chalcones and Application to Total Synthesis

Akira Nakamura

YAKUGAKU ZASSHI, 2023, 143, 105
DOI: 10.1248/yakushi.22-00154

One-pot green synthesis, biological evaluation, and in silico study of pyrazole derivatives obtained from chalcones

Emma Ghazaryan, Armen Karapetyan, Yana Gharibyan, Tigran Gharibyan, Asya Vorskanyan, Siranush Harutyunyan, Margarita Dovlatyan, Aleksandr Yengoyan and Tiruhi Gomktsyan

Green Processing and Synthesis, 2024, 13
DOI: 10.1515/gps-2024-0105

Hypervalent Iodine(III)‐Mediated 1,2‐Aryl Migration in 3‐Arylideneindolin‐2‐ones: A Route to 3‐Aryloxindole Derivatives

Prashik M. Walke, Aditya R. Narnawre, Karuna H. Shahani and Nandkishor N. Karade

ChemistrySelect, 2025, 10
DOI: 10.1002/slct.202405821

Oxidative Rearrangement of Secondary Amines Using Hypervalent Iodine(III) Reagent

Kenichi Murai, Tetsuya Kobayashi, Makoto Miyoshi and Hiromichi Fujioka

Org. Lett., 2018, 20, 2333
DOI: 10.1021/acs.orglett.8b00675

A Triazole‐Substituted Aryl Iodide with Omnipotent Reactivity in Enantioselective Oxidations

Ayham H. Abazid and Boris J. Nachtsheim

Angewandte Chemie, 2020, 132, 1495
DOI: 10.1002/ange.201912023

Oxidative Rearrangement of 3-Aminoindazoles for the Construction of 1,2,3-Benzotriazine-4(3H)-ones at Ambient Temperature

Yao Zhou, Ya Wang, Yixian Lou and Qiuling Song

Org. Lett., 2018, 20, 6494
DOI: 10.1021/acs.orglett.8b02813

n-Bu4NI/H2O2-catalyzed mild conversion of hydroxamic acids to carboxylic acids

Akira Nakamura, Jyunya Morimoto, Maho Taniguchi, Haruka Aoyama, Jiadong He and Tomohiro Maegawa

Tetrahedron Letters, 2023, 126, 154656
DOI: 10.1016/j.tetlet.2023.154656

A Triazole‐Substituted Aryl Iodide with Omnipotent Reactivity in Enantioselective Oxidations

Ayham H. Abazid and Boris J. Nachtsheim

Angew Chem Int Ed, 2020, 59, 1479
DOI: 10.1002/anie.201912023

Bifunctionalization of α,β-unsaturated diaryl ketones into α-aryl-β,β-ditosyloxy ketones: Single crystal XRD, DFT, FMOs, molecular electrostatic potential, hirshfeld surface analysis, and 3D-energy frameworks

Ravinder Kumar, Raj Kamal, Vipan Kumar and Jai Parkash

Journal of Molecular Structure, 2022, 1250, 131754
DOI: 10.1016/j.molstruc.2021.131754

Synthesis, XRD and Mechanistic Studies of α‐Aryl‐β,β‐ditosyloxy Ketones: An Oxidative 1,2‐Aryl Migration in α,β‐Unsaturated Diaryl Ketones Under Metal Free Conditions

Ravinder Kumar, Jai Parkash, Raj Kamal, Vipan Kumar and Sangeeta Saini

Asian J Org Chem, 2022, 11
DOI: 10.1002/ajoc.202100578

In Situ Hypoiodite-Catalyzed Oxidative Rearrangement of Chalcones: Scope and Mechanistic Investigation

Meiqiong Zheng, Chao Huang, Jian-Zhong Yan, Shu-Li Xie, Shao-Jia Ke, Hai-Dong Xia and Ya-Nan Duan

J. Org. Chem., 2023, 88, 1504
DOI: 10.1021/acs.joc.2c02291

Recent Progress in Synthetic Applications of Hypervalent Iodine(III) Reagents

Akira Yoshimura and Viktor V. Zhdankin

Chem. Rev., 2024, 124, 11108
DOI: 10.1021/acs.chemrev.4c00303

Deprotection of the Carbazole PMB Group Using Hypervalent Iodine Reagent Combined with N-Hydroxyphthalimide

Tomohiro Maegawa, Kana Yoshikawa, Takanori Tabata, Kazuma Fujimura, Natsumi Kuraoka, Akira Nakamura and Yasuyoshi Miki

HETEROCYCLES, 2021, 103, 1031
DOI: 10.3987/COM-20-S(K)46