Trifluoromethyl-substituted selenium ylide: a broadly applicable electrophilic trifluoromethylating reagent

2019 ◽  
Vol 6 (13) ◽  
pp. 2205-2209 ◽  
Author(s):  
Hangming Ge ◽  
Qilong Shen

An easily available, air/moisture insensitive and broadly applicable electrophilic reagent trifluoromethyl-substituted selenium ylide 1a and its reactions with a variety of nucleophiles including β-ketoesters and silyl enol ethers, aryl/heteroaryl boronic acids, electron-rich heteroarenes and sulfinates were described.

Synlett ◽  
2019 ◽  
Vol 30 (13) ◽  
pp. 1525-1535 ◽  
Author(s):  
Zhe Zhou ◽  
László Kürti

In this account, we provide an overview of some recent advances in electrophilic amination methodologies that have been developed in the Kürti group over the last seven years. Our group’s focus has been to develop novel amination methodologies that directly yield N-unprotected amine products.1 Introduction2 Amination of Boronic Acids3 Aziridination of Unactivated Olefins4 Rhodium-Catalyzed C–H Amination of Arenes5 Synthesis of Carbazoles6 Amination of Aryl- and Alkylmetals7 Doubly Electrophilic N-Linchpin Reagents8 Aza-Rubottom Oxidation of Silyl Enol Ethers9 Summary


2014 ◽  
Vol 18 (5) ◽  
pp. 525-546 ◽  
Author(s):  
Carmen Hernandez-Cervantes ◽  
Miriam Alvarez-Corral ◽  
Manuel Munoz-Dorado ◽  
Ignacio Rodriguez-Garcia

Author(s):  
Kohsuke Aikawa ◽  
KyoKo Nozaki ◽  
Takashi Okazoe ◽  
Yuichiro Ishibashi ◽  
Akiya Adachi

ChemInform ◽  
2010 ◽  
Vol 23 (48) ◽  
pp. no-no
Author(s):  
E. C. ROOS ◽  
H. HIEMSTRA ◽  
W. N. SPECKAMP ◽  
B. KAPTEIN ◽  
J. KAMPHUIS ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 28 (38) ◽  
pp. no-no
Author(s):  
S. PONTHIEUX ◽  
F. OUTURQUIN ◽  
C. PAULMIER

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