Ξ€_Publications_2019
Publications
2005
2006
2007
2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018 2019
2020
2021
2022
2023
2024
15.
Novel Development of Umpolung at Main Group Element: Synthesis,
Structure and Reactivity of Nucleophilic Aluminyl Anion
Takuya Kodama
J.
Synth. Org. Chem. Jpn.
2019,
77(12),
1247–1249.(Review
de Debut)
https://doi.org/10.5059/yukigoseikyokaishi.77.1247
14.
Oxovanadium(V)-catalyzed
deoxygenative homocoupling reaction of alcohols
Takashi Sakuramoto, Yosuke Donaka,
Mamoru Tobisu,
and Toshiyuki
Moriuchi
New J. Chem.,
in press.
http://dx.doi.org/10.1039/c9nj01905g
13.
Linear [3]Spirobifluorenylene: An S-Shaped Molecular Geometry of
p-Oligophenyls
Jumpei Oniki, Toshiyuki Moriuchi, Kosuke Kamochi,
Mamoru Tobisu,
and
Toru Amaya
J. Am. Chem. Soc.,
141 (45), 18238-18245 (2019).
http://dx.doi.org/10.1021/jacs.9b09179
12.
Recent Advances in Gomberg-Bachmann Biaryl Synthesis
Toru Amaya, Yuqing Jin,
and Mamoru Tobisu
Tetrahedron Lett..,
60 (39), 151062 (2019). (Digest review).
http://dx.doi.org/10.1016/tetlet.2019.151062
11.
N]Heterocyclic
Carbene]Catalyzed
Concerted Nucleophilic Aromatic Substitution of Aryl Fluorides Bearing
Ώ,ΐ]Unsaturated
Amides
Kosuke Yasui, Miharu Kamitani,
and Mamoru Tobisu
Angew. Chem. Int. Ed.,
58
(40),
14157-14161 (2019).
http://dx.doi.org/10.1002/anie.201907837
10.
Iridium-Mediated Arylation of Quinoline via the Cleavage of Carbon-Carbon
and Carbon-Nitrogen Bonds of 1,3-Dimesitylimidazol-2-ylidene
Shun Sakurai
and Mamoru Tobisu
Organometallics,
38 (14),
2834-2838
(2019).
http://dx.doi.org/10.1021/acs.organomet.9b00338
9.
Nichel-Catalized Decarbonylation of N-Acylated N-Heteroarenes
Toshifumi Morioka, Syun Nakatani, Yuki Sakamoto,
Takuya
Kodama,
Sensuke Ogoshi,
Naoto Chatani, and Mamoru Tobisu
Chem. Sci.,
10,
6666-6671
(2019).
http://dx.doi.org/10.1039/c9sc02035g
8.
Thiolate-Induced Synthesis of Dibenzothiophenes from
2,2'-Bis(methylthio)-1,1'-Biaryl Derivatives via
the Cleavage of Two Carbon-Sulfur Bonds
Yoshihiro Masuya, Yuki Kawashima,
Takuya
Kodama,
Naoto Chatani, and Mamoru Tobisu
Synlett,
30 (17), 1995-1999
(2019)
(Invited contribution to Cluster on Metathesis).
http://dx.doi.org/10.1055/s-0037-1611974
7.
Cyclization of Bisphosphines to Phosphacycles via the Cleavage of Two
Carbon–Phosphorus Bonds by Nickel Catalysis
Hayato Fujimoto, Momoka
Kusano, Takuya
Kodama, and Mamoru Tobisu
Org. Lett.,
21(11)
4177-4181
(2019).
http://dx.doi.org/10.1021/acs.orglett.9b01355
6.
Nickel-Catalyzed Decarboxylation of Aryl Carbamates for Converting
Phenols into Aromatic Amines
Akihiro Nishizawa, Tsuyoshi Takahira, Kosuke Yasui, Hayato Fujimoto, Tomohiro Iwai, Masaya Sawamura , Naoto Chatani, and Mamoru Tobisu
J. Am. Chem.
Soc.,
141(18)
7261-7265
(2019).
http://dx.doi.org/10.1021/jacs.9b02751
5.
Synthesis of a Sumanenyl Hafnocene Complex
Toru Amaya, Shun Katoh, Toshiyuki Moriuchi, and Toshikazu Hirao
Org. Chem. Front., 6(7) 1032-1037 (2019).
This article is part of the themed collection: In celebration of Julius
Rebekfs 75th Birthday.
http://dx.doi.org/10.1030/c9qo00140a
4.
Metal-Catalyzed Aromatic C-O Bond Activation/Transformation
Mamoru Tobisu
and
Naoto Chatani
In Organometallics
for Green Catalysis. Topics in Organometallic Chemistry, vol 63.; Pierre
H. Dixneuf, Jean-Francois Soule Eds.; Springer: Cham, 2018; pp103-140.
http://dx.doi.org/10.1007/3418_2018_19
3.
Oxovanadium(V)]Catalyzed
Direct Amination of Allyl Alcohols
Takashi Sakuramoto, Toshikazu
Hirao, Mamoru Tobisu,
and
Toshiyuki Moriuchi
ChemCatChem,
11(4),
1175-1178
(2019).
(Selected as a "Cover Feature").
http://dx.doi.org/10.1002/cctc.201801841
2.
Nickel-Catalyzed Cross-Coupling of 2- Methoxynaphthalene with Methyl
4-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzoate
Yuki Kawashima, Takayuki Furukawa,
Naoto Chatani,
and
Mamoru
Tobisu
Org. Synth.,
96,
36-52
(2019).
http://dx.doi.org/10.15227/orgsyn.096.0036
1.
Iridium-catalyzed
Decarbonylative Coupling of Acyl Fluorides with Arenes and Heteroarenes
via C-H Activation
Shun Sakurai,
Tomoki Yoshida, and
Mamoru
Tobisu
Chem.
Lett.,
48(1),
94-97
(2019).
http://dx.doi.org/10.1246/cl.180857
±Μy[WΜgbv
2018 2020
Copyright(c)All right reserved. The Tobisu
Group.