研究成果/ Publications

  • 原著論文 / Original Article
  • 総説論文 / Review Article


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2022

Reductive Dimerization of Styrenes to 1,4-Organodilithiums Enabled by Flow Microreactors

Yiyuan Jiang, and Hideki Yorimitsu*

ChemRxiv 2022.

DOI: 10.26434/chemrxiv-2022-6h3l7

Late-stage sulfonic acid/sulfonate formation from sulfonamides via sulfonyl pyrroles

Tomoya Ozaki, Hideki Yorimitsu*, and Gregory J.P. Perry*

Tetrahedron 2022, 117-118, 132830.

DOI: 10.1016/j.tet.2022.132830


Regioselective anti-Silyllithiation of Propargylic Alcohols

Somnath N. Karad, Hayate Saito, Jun Shimokawa*, and Hideki Yorimitsu*

ChemRxiv 2022.

DOI: 10.26434/chemrxiv-2022-7frsl

Reductive anti-dimagnesiation and dialumination of alkynes: Synthesis and reactions of trans-1,2-dimetalloalkenes

Fumiya Takahashi, Takashi Kurogi, and Hideki Yorimitsu*

ChemRxiv 2022.

DOI: 10.26434/chemrxiv-2022-h72gz

Sodium Silylsilanolate as a Precursor of Silylcopper Species

Hiroki Yamagishi, Kenshiro Hitoshio, Jun Shimokawa*, and Hideki Yorimitsu*

Chem. Sci. 2022, 13, 4334-4340.

DOI: 10.1039/D2SC00227B


Reductive Ring-opening of Arylcyclopropanecarboxamides Accompanied by Borylation and Enolate Formation

Shuo Wang, Atsushi Kaga, Takashi Kurogi, and Hideki Yorimitsu*

Org. Lett. 2022, 24, 1105-1109.

DOI: 10.1021/acs.orglett.2c00084


Facile Multiple Alkylations of C60 Fullerene

Kazuhira Miwa, Shinobu Aoyagi*, Takahiro Sasamori*, Shogo Morisako, Hiroshi Ueno, Yutaka Matsuo, and Hideki Yorimitsu

Molecules 2022, 27, 450.

DOI: 10.3390/molecules27020450


AgF-Mediated Electrophilic Amination of Alkoxyarylsilanes with Azodicarboxylates

Qian Zhang, Shijun Deng, Dong Li*, Jun Shimokawa*, and Hideki Yorimitsu

Chem. Asian J. 2022, e202101345.

DOI: 10.1002/asia.202101345


Five-fold Symmetric Pentaindolo- and Pentakis(benzoindolo)-Corannulenes: Unique Structural Dynamics Derived from the Combination of Helical- and Bowl-Inversions

Koki Kise, Shota Ooi, Hayate Saito, Hideki Yorimitsu, Atsuhiro Osuka, and Takayuki Tanaka*

Angew. Chem. Int. Ed. 2022, 61, e202112589.

DOI: 10.1002/anie.202112589


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2015

Review

Sulfonium-aided coupling of aromatic rings via sigmatropic rearrangement

Hideki Yorimitsu* and Gregory J. P. Perry*

Proc. Jpn. Acad., Ser. B. 2022, 98, 190-205.

DOI: 10.2183/pjab.98.012


Sulfur(IV) in Transition-Metal-Free Cross-Couplings for Biaryl Synthesis

Gregory J. P. Perry* and Hideki Yorimitsu*

ACS Sustainable Chem. Eng. 2022, 10, 2569-2586.

DOI: 10.1021/acssuschemeng.1c08673


シグマトロピー転位を活用するビアリール合成の新展開
Recent Development of Biaryl Synthesis through Sigmatropic Rearrangement

Tomoyuki Yanagi and Hideki Yorimitsu*

J. Synth. Org. Chem. Jpn. 2021, 79, 427-438.

DOI: 10.5059/yukigoseikyokaishi.79.427


Catalytic Transformations of Sulfonium Salts via C-S Bond Activation

Hideki Yorimitsu*

Chem. Rec. 2021, 3356-3369.

DOI: 10.1002/tcr.202000172


Electron injection for aromatic metamorphosis of indole

Hideki Yorimitsu*

J. Chin. Chem. Soc. 2021, 68, 536-540.

DOI: 10.1002/jccs.202000369


Catalytic C–H Arylation of Tetrathiafulvalenes for the Synthesis of Functional Materials

Hideki Yorimitsu*, Aya Yoshimura, Yohji Misaki

Synthesis 2020, 52, 3326.

DOI: 10.1055/s-0040-1707256


Carbon–Carbon Bond Cleavage at Allylic Positions: Retro-allylation and Deallylation

Keisuke Nogi, and Hideki Yorimitsu*

Chem. Rev. 2021, 121, 345.

DOI: 10.1021/acs.chemrev.0c00157


Catalytic Carbonylation and Carboxylation of Organosulfur Compounds via C–S cleavage

Keisuke Nogi*, and Hideki Yorimitsu*

Chem. Asian J. 2020, 15, 441-449.

DOI: 10.1002/asia.201901644


Ring-expanding and Ring-opening Transformations of Benzofurans and Indoles with Introducing Heteroatoms

Hayate Saito, and Hideki Yorimitsu*

Chem. Lett. 2019, 48, 1019–1028.

DOI: 10.1246/cl.190393


Catalytic inter- and intramolecular coupling of aryl sulfones

Fumiya Takahashi, Keisuke Nogi, and Hideki Yorimitsu*

Phosphorus Sulfur Silicon Relat. Elem. 2019, 194, 742–745.

DOI: 10.1080/10426507.2019.1603232


Recent development of ortho-C–H functionalization of aryl sulfoxides through [3,3] sigmatropic rearrangement

Tomoyuki Yanagi, Keisuke Nogi, and Hideki Yorimitsu*

Tetrahedron Lett. 2018, 59, 2951-2959.

DOI: 10.1016/j.tetlet.2018.06.055


C–S Bond Activation

Shinya Otsuka, Keisuke Nogi, and Hideki Yorimitsu*

Top. Curr. Chem. 2018, 376, 13.

DOI: 10.1007/s41061-018-0190-7


Cascades of Interrupted Pummerer Reaction-Sigmatropic Rearrangement

Hideki Yorimitsu*

Chem. Rec. 2017, 17, 1156–1167.

DOI: 10.1002/tcr.201700017


Aromatic metamorphosis: conversion of an aromatic skeleton into a different ring system

Keisuke Nogi, and Hideki Yorimitsu*

Chem. Commun. 2017, 53, 4055–4065.

DOI: 10.1039/C7CC00078B

Highlighted as Cover Picture.

Cross-coupling of Aryl Sulfides Powered by N-Heterocyclic Carbene Ligands

Ke Gao, Shinya Otsuka, Alexandre Baralle, Keisuke Nogi, Hideki Yorimitsu*, and Atsuhiro Osuka

J. Synth. Org. Chem. Jpn. 2016 74 1119–1127.

DOI: 10.5059/yukigoseikyokaishi.74.1119


Aromatic Metamorphosis of Dibenzothiophenes

Hideki Yorimitsu*, Dhananjayan Vasu, M. Bhanuchandra, Kei Murakami, and Atsuhiro Osuka

Synlett 2016, 27, 1765–1774.

DOI: 10.1055/s-0035-1561617