diallyl ether
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Author(s):  
Tamanna Poonia ◽  
Weslley G. D. P. Silva ◽  
Jennifer van Wijngaarden

Rotational spectroscopy and quantum mechanical calculations reveal a significant change in conformational landscapes when oxygen is substituted with sulfur: observation of features from nine conformers of diallylether versus one of the sulfide.


Molecules ◽  
2021 ◽  
Vol 26 (23) ◽  
pp. 7322
Author(s):  
Jérémy Ternel ◽  
Adrien Lopes ◽  
Mathieu Sauthier ◽  
Clothilde Buffe ◽  
Vincent Wiatz ◽  
...  

Isosorbide and its functionalized derivatives have numerous applications as bio-sourced building blocks. In this context, the synthesis of diols from isosorbide diallyl ether by hydrohydroxymethylation reaction is of extreme interest. This hydrohydroxymethylation, which consists of carbon-carbon double bonds converting into primary alcohol functions, can be obtained by a hydroformylation reaction followed by a hydrogenation reaction. In this study, reductive hydroformylation was achieved using isosorbide diallyl ether as a substrate in a rhodium/amine catalytic system. The highest yield in bis-primary alcohols obtained was equal to 79%.


2016 ◽  
Vol 118 (2) ◽  
pp. 719-731 ◽  
Author(s):  
A. Wróblewska ◽  
E. Drewnowska ◽  
A. Gawarecka

2015 ◽  
Vol 127 (52) ◽  
pp. 16071-16075 ◽  
Author(s):  
Zhongbao Jian ◽  
Stefan Mecking
Keyword(s):  

2015 ◽  
Vol 54 (52) ◽  
pp. 15845-15849 ◽  
Author(s):  
Zhongbao Jian ◽  
Stefan Mecking
Keyword(s):  

2015 ◽  
Vol 797 ◽  
pp. 347-351 ◽  
Author(s):  
Ewa Drewnowska ◽  
Agnieszka Wróblewska ◽  
Alicja Gawarecka

This work presents the research on the influence of the addition of the appropriate amounts of the inorganic salt (Na2SO4) on the reduction of the ineffective decomposition of hydrogen peroxide (H2O2) and simultaneously on the increase of the efficiency of hydrogen peroxide conversion. The studies were carried out for the epoxidation of diallyl ether to allyl-glycidyl ether with 30 wt% hydrogen peroxide on the TS-1 catalyst and in the presence of acetonitrile as the solvent. The studies were conducted in the following conditions: the temperature of 70°C, the molar ratio of diallyl ether/hydrogen peroxide = 3:1, the acetonitrile concentration of 50 wt%, the TS-1 content of 9 wt%, the reaction time of 3 hours, the intensity of stirring of 500 rpm and the molar ratio of hydrogen peroxide/Na2SO42:1 to 14:1 (also the results for epoxidation of diallyl ether without Na2SO4were presented)


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