鳶巣研_Publications_2022
Publications
2005
2006
2007
2008
2009
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2011
2012
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2014
2015
2016
2017
2018
2019
2020
2021 2022
2023
2024
15. Nickel-Catalyzed
Cross Coupling via C–O
and C–N
Activation
Tomoki Yoshida and Mamoru Tobisu
Science of Synthesis: Base-Metal Catalysis,
2022,
1,
591–630.
https://www.thieme-connect.com/products/ebooks/lookinside/10.1055/sos-SD-238-00298
14. Zn(II)-catalyzed
Formal Cross-Dimerization of Carbenes Using Acylsilanes and Diazo Esters
Tomoki Yoshida, Masaya Ohta, Tomoya Emmei, Takuya Kodama, and Mamoru
Tobisu
Chem. Lett.,
2023, 52(1), 48–50.
https://doi.org/10.1246/cl.220476
13. Rhodium-catalyzed
Decarbonylation of Acylsilanes
Tomoki Yoshida, Takuya Kodama, and Mamoru Tobisu
Asian J. Org. Chem.,
2022, 11(12), e202200610. (Invited contribution to the
special collection on the occasion of Professor Keiji Maruoka's 70th
birthday)
https://doi.org/10.1002/ajoc.202200610
12. Pd-catalyzed
siloxycyclopropanation of alkenes
Shun Sakurai,
Tetsuya Inagaki, Takuya Kodama, Masahiro Yamanaka,
and Mamoru Tobisu
Trends in Chemistry,
2022,
4(12),
1161–1162.
(Invited contribution to 'Mechanism of the Month')
https://doi.org/10.1016/j.trechm.2022.08.011
11. Phosphine-Catalyzed
Z-Selective Carbofluorination of Alkynoates Bearing an N-Heteroarene
Units
Hayato Fujimoto, Shisato Yamamura, Namiki Takenaka, and Mamoru Tobisu
Synthesis,
2022, in press
(Invited contribution to the special issue on 'Synthetic Advancements
Enabled by Phosphorus Redox Chemistry')
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/a-1948-3234
10. Synthetic
Applications of C–O and C–E Bond Activation Reactions
Mamoru Tobisu, Takuya Kodama and Hayato Fujimoto
In
Comprehensive Organometallic Chemistry IV,
2022,
12,
pp347–420.
https://www.sciencedirect.com/science/article/pii/B9780128202067000895
9. Nickel-catalyzed
1,4-aryl rearrangement of aryl N-benzylimidates via C–O and C–H
bond cleavage
Satoshi Ogawa and Mamoru Tobisu
Chem. Commun.,
2022,
58(57),
7909–7911.
https://doi.org/10.1039/d2cc02355
8. Palladium-Catalyzed
Unimolecular Fragment Coupling of N-Allylamides via Elimination
of Isocyanate
Ryoma Shimazumi, Riku Tanimoto,
Takuya Kodama, and Mamoru Tobisu
J.
Am. Chem. Soc.,
2022,
144(24),
11033–11043.
https://doi.org/10.1021/jacs.2c04527
7. Non-Stabilized
Vinyl Anion Equivalents from Styrenes by N-Heterocyclic Carbene
Catalysis and Its Use in Catalytic Nucleophilic Aromatic Substitution
Sora Ito, Hayato Fujimoto,
and Mamoru Tobisu
J.
Am. Chem. Soc.,
2022,
144(15),
6714–6718.
https://doi.org/10.1021/jacs.2c02579
6. Nickel-Catalyzed
Skeletal Transformation of Tropone Derivatives via C–C Bond Activation:
Catalyst-Controlled Access to Diverse Ring Systems
Takuya Kodama, Kanako Saito,
and Mamoru Tobisu
Chem. Sci.,
2022, 13(17),
4922–4929.
https://doi.org/10.1039/D2SC01394K
5. Palladium-Catalyzed
Silylacylation of Allenes Using Acylsilanes
Tetsuya Inagaki, Shun Sakurai, Masahiro Yamanaka,
and Mamoru Tobisu
Angew. Chem. Int. Ed.,
2022, 61(21), e202202387.
https://doi.org/10.1002/anie.202202387
4. Overlooked
Factors Required for Electrolyte Solvents in Li–O₂ Batteries:
Capabilities of Quenching 1O₂ and Forming Highly-Decomposable
Li₂O₂
Kiho Nishioka, Mizuki Tanaka, Hayato Fujimoto, Toru Amaya, Sensuke
Ogoshi, Mamoru Tobisu, and Shuji Nakanishi
Angew. Chem. Int. Ed.,
2022, 61(12), e202112769.
https://doi.org/10.1002/anie.202112769
3. Ratiometric
and colorimetric detection of Cu2+ via the oxidation of
benzodihydroquinoline derivatives and related synthetic methodology
Waroton Paisuwan, Vachiraporn
Ajavakom, Mongkol Sukwattanasinitt, Mamoru Tobisu, Anawat Ajavakom
Sens. Bio-Sens. Res.,
2022,
35,
100470.
https://doi.org/10.1016/j.sbsr.2021.100470
2. Palladium-Catalyzed
Siloxycyclopropanation of Alkenes Using Acylsilanes
Shun Sakurai, Tetsuya Inagaki, Takuya Kodama, Masahiro Yamanaka,
and Mamoru Tobisu
J.
Am. Chem. Soc.,
2022,
144(3),
1099–1105.
https://pubs.acs.org/doi/10.1021/jacs.1c11497
1. Nickel-Catalyzed
Addition of C–C Bonds of Amides to Strained Alkenes: The
1,2-Carboaminocarbonylation Reaction
Yuri Ito, Syun Nakatani, Ryota
Shiraki, Takuya Kodama, and Mamoru Tobisu
J.
Am. Chem. Soc.,
2022,
144(2),
662–666.
https://pubs.acs.org/doi/10.1021/jacs.1c09265
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