Regioselective synthesis of halohydrin esters from epoxides: reaction with acyl halides and rhodium-catalyzed three-component coupling reaction with alkyl halides and carbon monoxide

2009 ◽  
pp. 6970 ◽  
Author(s):  
Koji Nakano ◽  
Shunsuke Kodama ◽  
Yessi Permana ◽  
Kyoko Nozaki
2004 ◽  
Vol 346 (8) ◽  
pp. 905-908 ◽  
Author(s):  
Jun Terao ◽  
Shinsuke Nii ◽  
Firoz A. Chowdhury ◽  
Akifumi Nakamura ◽  
Nobuaki Kambe

2020 ◽  
Vol 56 (66) ◽  
pp. 9513-9516
Author(s):  
Fei Li ◽  
Yanbo Shang ◽  
Chuang Niu ◽  
Chao Li ◽  
Xinmin Huang ◽  
...  

An efficient one-pot three-component domino coupling reaction of phenols, C60, and bromoalkanes was developed, resulting in the highly regioselective synthesis of 1,4-asymmetrical C60 bisadducts.


Author(s):  
Takahide Fukuyama ◽  
Md Taifur Rahman ◽  
Naoya Kamata ◽  
Ilhyong Ryu

Radical-based carbonylation reactions of alkyl halides were conducted in a microflow reactor under pressurized carbon monoxide gas. Good to excellent yields of carbonylated products were obtained via radical formylation, carbonylative cyclization and three-component coupling reactions, using tributyltin hydride or TTMSS as a radical mediator.


2003 ◽  
Vol 5 (21) ◽  
pp. 3959-3961 ◽  
Author(s):  
Keiya Mizutani ◽  
Hiroshi Shinokubo ◽  
Koichiro Oshima

ChemInform ◽  
2010 ◽  
Vol 23 (34) ◽  
pp. no-no
Author(s):  
Y. TAMARU ◽  
K. YASUI ◽  
H. TAKANABE ◽  
S. TANAKA ◽  
K. FUGAMI

1992 ◽  
Vol 31 (5) ◽  
pp. 645-646 ◽  
Author(s):  
Yoshinao Tamaru ◽  
Kengo Yasui ◽  
Hidenobu Takanabe ◽  
Shuji Tanaka ◽  
Keigo Fugami

Synthesis ◽  
2020 ◽  
Vol 52 (22) ◽  
pp. 3466-3472
Author(s):  
Yunkui Liu ◽  
Bingwei Zhou ◽  
Qiao Li ◽  
Hongwei Jin

We herein describe a Ni-catalyzed multicomponent coupling reaction of alkyl halides, isocyanides, and H2O to access alkyl amides. Bench-stable NiCl2(dppp) is competent to initiate this transformation under mild reaction conditions, thus allowing easy operation and adding practical value. Substrate scope studies revealed a broad functional group tolerance and generality of primary and secondary alkyl halides in this protocol. A plausible catalytic cycle via a SET process is proposed based on preliminary experiments and previous literature.


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