One-pot synthesis of α-trifluoromethylstyrenes from aryl ketones and the Ruppert–Prakash reagent

2021 ◽  
Vol 31 (5) ◽  
pp. 684-685
Author(s):  
Vitalij V. Levin ◽  
Alexander D. Dilman
SynOpen ◽  
2019 ◽  
Vol 03 (04) ◽  
pp. 138-141
Author(s):  
Man Lung D. Kwan ◽  
Paul R. Challen ◽  
Quynh D.-D. Tran

A convenient one-pot synthesis of allylsilanes from enolizable methyl aryl ketones has been developed. The first step involves nucleophilic addition of the trimethylsilylmethyl group to ketones using the alkylation method developed by Ishihara with slight modification to generate the corresponding β-silylalkoxides. The second step entails addition of diisobutylaluminum chloride and heating at about 130 °C overnight to afford allylsilanes in fair yields.


2015 ◽  
Vol 39 (11) ◽  
pp. 8763-8770 ◽  
Author(s):  
Md Yousuf ◽  
Tuluma Das ◽  
Susanta Adhikari

The versatile, one-pot synthesis of a series of alkyl aryl ketones is described using ethyl cyanoacetate as a new acylating agent.


2019 ◽  
Vol 84 (9) ◽  
pp. 5141-5149 ◽  
Author(s):  
Wenqiang Jia ◽  
Qiumu Xi ◽  
Tianqi Liu ◽  
Minjian Yang ◽  
Yonghui Chen ◽  
...  

2015 ◽  
Vol 17 (19) ◽  
pp. 4850-4853 ◽  
Author(s):  
Yusuke Hara ◽  
Shunsuke Onodera ◽  
Takuya Kochi ◽  
Fumitoshi Kakiuchi

2016 ◽  
Vol 14 (3) ◽  
pp. 858-861 ◽  
Author(s):  
Mahesh H. Shinde ◽  
Umesh A. Kshirsagar

An N-Bromosuccinimide (NBS) promoted one pot strategy for the synthesis of α-amino functionalized aryl ketones starting from commercially available styrenes has been developed.


ChemInform ◽  
2016 ◽  
Vol 47 (7) ◽  
pp. no-no
Author(s):  
Yusuke Hara ◽  
Shunsuke Onodera ◽  
Takuya Kochi ◽  
Fumitoshi Kakiuchi

2021 ◽  
Vol 19 (6) ◽  
pp. 1386-1394
Author(s):  
Shaikh Samser ◽  
Priyabrata Biswal ◽  
Sushanta Kumar Meher ◽  
Krishnan Venkatasubbaiah

Synthetically important 3-aryl substituted cyclohexenones or 1,5-diketones were prepared from arylketones and allyl alcohols using a palladium-BINOL phosphoric acid system.


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