Junichiro Yamaguchi
Affiliations: | Waseda University, Shinjuku-ku, Tōkyō-to, Japan |
Area:
Organic synthesisGoogle:
"Junichiro Yamaguchi"Mean distance: (not calculated yet)
Parents
Sign in to add mentorYujiro Hayashi | grad student | 2001-2007 | Tohoku University |
Phil S. Baran | post-doc | 2007-2008 | Scripps Institute |
Children
Sign in to add traineeRyota Isshiki | grad student | 2016-2022 | Hokkaido University |
Hugo Ohki | grad student | 2021-2027 | Waseda University |
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Publications
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Uehara TN, Takao S, Matsuo H, et al. (2023) A small molecule modulator affecting clock-associated PSEUDO-RESPONSE REGULATOR 7 amount. Plant & Cell Physiology |
Miyazaki R, Muto K, Yamaguchi J. (2023) Chloroacetyl boronate -tosylhydrazone as a versatile synthetic building block. Chemical Communications (Cambridge, England). 59: 7419-7422 |
Komatsuda M, Yamaguchi J. (2023) Ring-opening Fluorination of Carbo/Heterocycles and Aromatics: Construction of Complex and Diverse Fluorine-containing Molecules. Chemical Record (New York, N.Y.). e202200281 |
Kurosawa MB, Kato K, Muto K, et al. (2022) Unified synthesis of multiply arylated alkanes by catalytic deoxygenative transformation of diarylketones. Chemical Science. 13: 10743-10751 |
Nakahara H, Yamaguchi J. (2022) Aryl Dance Reaction of Arylbenzoheteroles. Organic Letters. 24: 8083-8087 |
Iizumi K, Nakayama KP, Kato K, et al. (2022) Synthesis and Properties of Pyridine-Fused Triazolylidene-Palladium: Catalyst for Cross-Coupling Using Chloroarenes and Nitroarenes. The Journal of Organic Chemistry. 87: 11909-11918 |
Wu Q, Muto K, Yamaguchi J. (2022) Pd-Catalyzed 1,4-Carboamination of Bicyclic Bromoarenes with Diazo Compounds and Amines. Organic Letters. 24: 4129-4134 |
Kubo M, Inayama N, Ota E, et al. (2022) Palladium-Catalyzed Tandem Ester Dance/Decarbonylative Coupling Reactions. Organic Letters |
Komatsuda M, Ohki H, Kondo H, et al. (2022) Ring-Opening Fluorination of Isoxazoles. Organic Letters. 24: 3270-3274 |
Nie YH, Komatsuda M, Yang P, et al. (2022) Pd-Catalyzed Asymmetric Dearomative Arylation of Indoles via a Desymmetrization Strategy. Organic Letters |