Ξ€_Publications_2019
	
	
		
		
		 
		
				
		
 
		
 
 
		
 
		
 
 
		
 
		

		 
		Publications
		
			
			2005 
		2006 
		2007 
		2008 
		2009 
		2010
		2011 
		2012
		2013
		2014 
		2015
		2016
		2017
		2018 2019
		2020
		2021
		2022
		2023
		2024
		2025
		
		
		
		
		
		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.