Publication

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145. Aryl Dance Reaction of Arylheteroles

Nakahara, H; Yamaguchi, J.
ChemRxiv. 2022, preprint
DOI 10.26434/chemrxiv-2022-bl6rx

144. Activation of Alkyl Chlorides Enabled by Zirconocene and Photoredox Catalysis

Okita, T.; Aida, K.; Tanaka, K.; Ota, E.; Yamaguchi, J.
ChemRxiv. 2022, preprint
DOI 10.26434/chemrxiv-2022-5n811

143. A unique small molecule pair controls the plant circadian clock

Uehara, T. N.; Takao, S.; Matsuo, H.; Saito, A.N.; Ota, E.; Ono, A.; Itami, K.; Kinoshita, T.; Yamaguchi, J.; Nakamichi, N.
BioRxiv. 2020, preprint
DOI 10.1101/2020.05.25.113746

New Publication

142. Structure-Function Study of a Novel Inhibitor of Cyclin-Dependent Kinase C in Arabidopsis

Saito, A. N.; Maeda, A. E.; Takahara, T. T.; Matsuo, H.; Nishina, M.; Ono, A.; Shiratake, K.; Notaguchi, M.; Yanai, T.; Kinoshita, T.; Ota, E.; Fujimoto, K. J.; Yamaguchi, J.; Nakamichi, N.
Plant Cell Physiol 2022. Just Accepted article.
DOI 10.1093/pcp/pcac127

141. Synthesis and Properties of Pyridine-Fused Triazolylidene–Palladium: Catalyst for Cross-Coupling Using Chloroarenes and Nitroarenes

Iizumi, K.; Nakayama, K. P.; Kato, K.; Muto, K.; Yamaguchi, J.
J. Org. Chem. 2022, 87, 11909–11918.
DOI 10.1021/acs.joc.2c01562
ChemRxiv. 2022, preprint
DOI 10.26434/chemrxiv-2022-qs9s9

140. Unified Synthesis of Multiply Arylated Alkanes by Catalytic Deoxygenative Transformation of Diarylketones

Kurosawa, M. B.; Kato, K.; Muto, K.; Yamaguchi, J.
Chem. Sci. 2022, 13, 10743 – 10751
DOI 10.1039/D2SC03720C
ChemRxiv. 2022, preprint
DOI 10.26434/chemrxiv-2022-h1860

139. Identification of α-Synuclein Proaggregator: Rapid Synthesis and Streamlining RT-QuIC Assays in Parkinson’s Disease

Takada, F.; Kasahara, T.; Otake, K.; Maru, T.; Miwa, M.; Muto, K.; Sasaki, M.; Hirozane, Y.; Yoshikawa, M; and Yamaguchi, J.
ACS Med. Chem. Lett. 2022, 13, 1421–1426.
DOI 10.1021/acsmedchemlett.2c00138

138. Chemical biology to dissect molecular mechanisms underlying plant circadian clocks

Nakamichi, N. Yamaguchi, J.; Sato, A.; Fujimoto, K. J. Ota, E.
New Phytologist 2022, 235, 1336–1343.
DOI 10.1111/nph.18298

137. Pd-Catalyzed 1,4-Carboamination of Bicyclic Bromoarenes with Diazo Compounds and Amines

Wu, Q.; Muto, K.; Yamaguchi, J.
Org. Lett. 2022, 24, 4129–4134
DOI 10.1021/acs.orglett.2c01233
Highlights Most Read Article (July, 2022)
ChemRxiv. 2022, preprint
DOI 10.26434/chemrxiv-2022-s5vdz

136. Palladium-Catalyzed Tandem Ester Dance/Decarbonylative Cou-pling Reactions

Kubo, M.; Inayama, N.; Ota, E.; Yamaguchi, J.
Org. Lett. 2022, 24, 3855–3860.
DOI 10.1021/acs.orglett.2c01432
Highlights Most Read Article (June, 2022)
ChemRxiv. 2022, preprint
DOI 10.26434/chemrxiv-2022-wfhc5

135. Decarbonylative Reductive Coupling of Aromatic Esters by Nickel and Palladium Catalyst

Peng, Y.; Isshiki, R.; Muto, K.; Yamaguchi, J.
Chem. Lett. 2022, 51, 749–753.
DOI 10.1246/cl.220214
ChemRxiv. 2022, preprint
DOI 10.26434/chemrxiv-2022-s0sxl

134. Catalytic reductive ring opening of epoxides enabled by zirconocene and photoredox catalysis

Aida, K.; Hirao, M.; Funabashi, A.; Sugimura, N.; Ota, E.; Yamaguchi, J.
Chem 2022, 8, 1762–1774.
DOI 10.1016/j.chempr.2022.04.010
Highlights Most Read Article (July, 2022)
Highlights Highlighted in Chem-Station, NIkkankogyo Shinbun
ChemRxiv. 2021, preprint
DOI 10.26434/chemrxiv.14605392.v1

133. Ring-Opening Fluorination of Isoxazoles

Komatsuda, M.; Ohki, H.; Kondo Jr., H.; Suto, A.; Yamaguchi, J.
Org. Lett. 2022, 24, 3270–3274
DOI 10.1021/acs.orglett.2c01149
ChemRxiv. 2022, preprint
DOI 10.26434/chemrxiv-2022-bj42g 

132. Formal Syntheses of Dictyodendrins B, C, and E by a Multi-substituted Indole Synthesis

Kabuki, A; Yamaguchi, J.
Synthesis, 2022, Just Accepted.
DOI 10.1055/a-1786-9881
ChemRxiv. 2021, preprint
DOI 10.26434/chemrxiv.14355812

131. Pd-Catalyzed Asymmetric Dearomative Arylation of Indoles via a Desymmetrization Strategy

Nie, Y.-H.; Komatsuda, M.; Yang, P.; Zheng, C.; Yamaguchi, J.; You, S.-L. .
Org. Lett. 2022, 24, 1481–1485.
DOI 10.1021/acs.orglett.2c00129

130. Phosphorylation of RNA Polymerase II by CDKC;2 Maintains the Arabidopsis Circadian Clock Period

Uehara, T. N.; Nonoyama, T.; Taki, K.; Kuwata, K.; Sato, A.; Fujimoto, K. J.; Hirota, T.; Matsuo, H.; Maeda, A. E.; Ono, A.; Takahara, T. T.; Tsutsui, H.; Suzuki, T.; Yanai, T.; Kay, S. A.; Itami, K.; Kinoshita, T.; Yamaguchi, J.; Nakamichi, N.
Plant Cell Physiol. 2022, 63, 450–462.
DOI 10.1093/pcp/pcac011

129. Ring-Opening Fluorination of Bicyclic Azaarenes

Komatsuda, M.; Suto, A.; Kondo Jr. H.; Takada, H.; Kato, K.; Saito, M.; Yamaguchi, J.
Chem. Sci. 2022, 13, 665–670.
DOI 10.1039/d1sc06273e
Highlights Selected as Cover picture
ChemRxiv. 2021, preprint
DOI 10.33774/chemrxiv-2021-gh325-v2

Representative Publications

  1. Komatsuda, M.; Suto, A.; Kondo Jr. H.; Takada, H.; Kato, K.; Saito, M.; Yamaguchi, J. Chem. Sci. 2022, 13, 665–670.
  2. Yanagimoto, A.;Uwabe, Y.; Wu, Q.; Muto, K.*; Yamaguchi, J. ACS Catal. 2021, 11, 10429¬–10435.
  3. Isshiki, R.; Kurosawa, M. B.; Muto, K.; Yamaguchi, J. J. Am. Chem. Soc. 2021, 143, 10333–10340.
  4. Kato, H.; Musha, I.; Komatsuda, M.; Muto, K.; Yamaguchi, J. Chem. Sci. 2020, 11, 8779 – 8784
  5. Matsushita, K.; Takise, R.; Muto, K.; Yamaguchi, J. Sci. Adv. 2020, 6, eaba7614.
  6. Kondo H.; Miyamura, S.; Matsushita, K.; Kato, H.; Kobayashi, C.: Arifin; Itami, K.; Yokogawa, D.; Yamaguchi, J. J. Am. Chem. Soc. 2020142, 11306–11313.
  7. Kurosawa, M. B.; Isshiki, R.; Muto, K.; Yamaguchi, J. J. Am. Chem. Soc. 2020, 142,7386–7392.
  8. Isshiki, R.; Inayama, N.; Muto, K.; Yamaguchi, J. ACS Catal. 2020, 10, 3490-3494.
  9. Ishitobi, K.; Muto, K.; Yamaguchi, J. ACS Catal. 2019, 9, 11685-11690.
  10. Komatsuda, M.; Kato, H.; Muto, K.; Yamaguchi, J. ACS Catal. 2019, 9, 8991–8995.
  11. Uehara, T. N.; Mizutani, Y.; Kuwata, K.; Hirota, T.; Sato, A.; Mizoi, J.; Takao, S.; Matsuo, H.; Suzuki, T.; Ito, S.; Saito, A. N.; Nishiwaki Ohkawa, T.; Yamaguchi-Shinozaki, K.; Yoshimura, T.; Kay, S. A.; Itami, K.; Kinoshita, T.; Yamaguchi, J.; Nakamichi, N. Proc Natl Acad Sci USA 2019,
  12. Suzuki, S.; Itami, K.; Yamaguchi, J. Angew. Chem., Int. Ed. 2017, 56, 15010.
  13. Takise, R.; Isshiki, R. Muto K.; Itami, K.; Yamaguchi, J. J. Am. Chem. Soc. 2017, 139, 3340.
  14. Muto K.; Yamaguchi, J.; Musaev, D.G.; Itami, K. Nature. Commun20156, 7508.
  15. Suzuki, S.; Segawa, Y.; Itami, K.; Yamaguchi, J. Nature Chem. 20157, 227.
  16. Yamaguchi, A. D.; Chepiga, K. M.; Yamaguchi, J.; Itami, K.; Davies, H. M. L. J. Am. Chem. Soc. 2015137, 644.
  17. Miyamura, S.; Araki, M.; Suzuki, T.; Yamaguchi, J.; Itami, K. Angew. Chem., Int. Ed. 201554, 846.
  18. Ueda, K.; Amaike, K.; Maceiczyk, R. M; Itami, K.; Yamaguchi, J. J. Am. Chem. Soc. 2014136, 13226.
  19. Takise, R.; Muto, K.; Yamaguchi, J.; J. Itami K. Angew. Chem., Int. Ed. 201453, 6791.
  20. Tani, S.; Uehara, T. N.; Yamaguchi, J.; Itami, K. Chem. Sci. 2014, 5, 123.
  21. Lingkui, M.; Kamada, Y.; Muto, K.; Yamaguchi, J.; Itami, K. Angew. Chem., Int. Ed. 2013, 52, 38, 10048.
  22. Amaike, K.; Muto, K.; Yamaguchi, J.; Itami, K. J. Am. Chem. Soc.2012134, 13573.
  23. Muto, K.; Yamaguchi, J.; Itami, K. J. Am. Chem. Soc. 2012134, 169.
  24. Mandal, D.; Yamaguchi, A. D.; Yamaguchi, J.; Itami, K. J. Am. Chem. Soc. 2011133, 19660.
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