scholarly journals Ni-Catalyzed Aryl Sulfide Synthesis through an Aryl Exchange Reaction

Author(s):  
Ryota Isshiki ◽  
Miki B. Kurosawa ◽  
Kei Muto ◽  
Junichiro Yamaguchi

A Ni-catalyzed aryl sulfide synthesis through an aryl exchange reaction between aryl sulfides and a variety of aryl electrophiles was developed. By using 2-pyridyl sulfide as a sulfide donor, this reaction achieved the synthesis of aryl sulfides without using odorous and toxic thiols. The use of a Ni/dcypt catalyst capable of cleaving and forming aryl–S bonds was important for the aryl exchange reaction between 2-pyridyl sulfides and aryl electrophiles, which include aromatic esters, arenol derivatives, and aryl halides. Mechanistic studies revealed that Ni/dcypt can simultaneously undergo oxidative additions of aryl sulfides and aromatic esters, followed by ligand exchange between the generated aryl–Ni–SR and aryl–Ni–OAr species to furnish aryl exchanged compounds.

2021 ◽  
Author(s):  
Ryota Isshiki ◽  
Miki B. Kurosawa ◽  
Kei Muto ◽  
Junichiro Yamaguchi

A Ni-catalyzed aryl sulfide synthesis through an aryl exchange reaction between aryl sulfides and a variety of aryl electrophiles was developed. By using 2-pyridyl sulfide as a sulfide donor, this reaction achieved the synthesis of aryl sulfides without using odorous and toxic thiols. The use of a Ni/dcypt catalyst capable of cleaving and forming aryl–S bonds was important for the aryl exchange reaction between 2-pyridyl sulfides and aryl electrophiles, which include aromatic esters, arenol derivatives, and aryl halides. Mechanistic studies revealed that Ni/dcypt can simultaneously undergo oxidative additions of aryl sulfides and aromatic esters, followed by ligand exchange between the generated aryl–Ni–SR and aryl–Ni–OAr species to furnish aryl exchanged compounds.


Author(s):  
Ryota Isshiki ◽  
Miki B. Kurosawa ◽  
Kei Muto ◽  
Junichiro Yamaguchi

2020 ◽  
Vol 33 (2) ◽  
pp. 210-216
Author(s):  
Björn Bastian ◽  
Tim Michaelsen ◽  
Milan Ončák ◽  
Jennifer Meyer ◽  
Roland Wester

Synlett ◽  
2017 ◽  
Vol 28 (11) ◽  
pp. 1258-1267 ◽  
Author(s):  
Hajime Ito ◽  
Eiji Yamamoto ◽  
Satoshi Maeda ◽  
Tetsuya Taketsugu

Silylboranes are used as borylation reagents for organohalides in the presence of alkoxy bases without transition-metal catalysts. PhMe2Si–B(pin) reacts with a variety of aryl, alkenyl, and alkyl halides, including sterically hindered examples, to provide the corresponding organoboronates in good yields with high borylation/silylation ratios, showing good functional group compatibility. Halogenophilic attack of a silyl nucleophile on organohalides, and subsequent nucleophilic attack on the boron electrophile are identified to be crucial, based on the results of extensive theoretical and experimental studies. This boryl­ation reaction is further applied to the first direct dimesitylboryl (BMes2) substitution of aryl halides using Ph2MeSi–BMes2 and Na(O-t-Bu), affording aryldimesitylboranes, which are regarded as an important class of compounds for organic materials.1 Introduction2 Boryl Substitution of Organohalides with PhMe2Si–B(pin)/Alkoxy Bases3 Mechanistic Investigations4 DFT Mechanistic Studies Using an Artificial Force Induced Reaction (AFIR) Method5 Dimesitylboryl Substitution of Aryl Halides with Ph2MeSi–BMes2/Na(O-t-Bu)6 Conclusion


2015 ◽  
Vol 17 (8) ◽  
pp. 5712-5724 ◽  
Author(s):  
W. J. Gerber ◽  
P.-H. van Wyk ◽  
D. M. E. van Niekerk ◽  
K. R. Koch

Bjerrum's model of step-wise ligand exchange is extended to compute a complete speciation diagram for the [PtCl6−nBrn]2−(n= 0–6) system including all 17 equilibrium constants concerning the PtIVchlorido–bromido exchange reaction network (HERN).


2011 ◽  
Vol 76 (11) ◽  
pp. 4371-4378 ◽  
Author(s):  
Namjin Park ◽  
Kyungho Park ◽  
Mihee Jang ◽  
Sunwoo Lee

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