2022(15)

143. Aryl Dance Reaction of Arybenzolheteroles

Nakahara, H; Yamaguchi, J.
Org. Lett. 2022, 24, 8083–8087
DOI 10.1021/acs.orglett.2c03442
Highlights Most Read Article (November, 2022)
ChemRxiv. 2022, preprint
DOI 10.26434/chemrxiv-2022-bl6rx

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, 63, 1720–1728,
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

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