scholarly journals One-pot synthesis of cyanohydrin derivatives from alkyl bromides via incorporation of two one-carbon components by consecutive radical/ionic reactions

2014 ◽  
Vol 10 ◽  
pp. 150-154 ◽  
Author(s):  
Shuhei Sumino ◽  
Akira Fusano ◽  
Hiroyuki Okai ◽  
Takahide Fukuyama ◽  
Ilhyong Ryu

The consecutive radical/ionic reaction consisting of radical formylation of alkyl bromides and nucleophilic addition of a cyanide ion was investigated, which gave moderate to good yields of cyanohydrin derivatives in one-pot.

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.


2011 ◽  
Vol 15 (4) ◽  
pp. 911-916 ◽  
Author(s):  
Zinatossadat Hossaini ◽  
Faramarz Rostami-Charati ◽  
Samira Soltani ◽  
Anwar Mirzaei ◽  
Kayhaneh Berijani

2012 ◽  
Vol 14 (9) ◽  
pp. 2202-2205 ◽  
Author(s):  
Kamal Nain Singh ◽  
Paramjit Singh ◽  
Pushpinder Singh ◽  
Yadwinder Singh Deol

2007 ◽  
Vol 4 (8) ◽  
pp. 567-570 ◽  
Author(s):  
Robabeh Baharfar ◽  
Seyed Baghbanian ◽  
Roghayeh Hossein nia ◽  
Hamid Bijanzadeh

Sign in / Sign up

Export Citation Format

Share Document