Efficient synthesis of cyclic carbonate from carbon dioxide catalyzed by polyoxometalate: the remarkable effects of metal substitution

2005 ◽  
Vol 233 (1) ◽  
pp. 119-122 ◽  
Author(s):  
H YASUDA ◽  
L HE ◽  
T SAKAKURA ◽  
C HU
2018 ◽  
Vol 54 (25) ◽  
pp. 3166-3169 ◽  
Author(s):  
Teemu Niemi ◽  
Israel Fernández ◽  
Bethany Steadman ◽  
Jere K. Mannisto ◽  
Timo Repo

Selective, straightforward, and efficient synthesis of cyclic carbamates from CO2 and amino alcohols.


2020 ◽  
Vol 10 (10) ◽  
pp. 3265-3278 ◽  
Author(s):  
Marta Navarro ◽  
Luis F. Sánchez-Barba ◽  
Andrés Garcés ◽  
Juan Fernández-Baeza ◽  
Israel Fernández ◽  
...  

The binuclear aluminum complexes [AlR2(κ2-NN′;κ2-NN′)AlR2] with TBAB/PPNCl behave as excellent systems for cyclic carbonate formation from CO2 with challenging epoxides.


2011 ◽  
Vol 121 (3) ◽  
pp. 1431-1441 ◽  
Author(s):  
Chikara Tsutsumi ◽  
Naohisa Fukukawa ◽  
Jun Sakafuji ◽  
Kazuyuki Oro ◽  
Kazuaki Hata ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (3) ◽  
pp. 2217-2224 ◽  
Author(s):  
Qingyuan Deng ◽  
Gaohong He ◽  
Yu Pan ◽  
Xuehua Ruan ◽  
Wenji Zheng ◽  
...  

Novel bis-ammonium immobilized polystyrenes with co-catalyzing functional groups were prepared for efficient synthesis of cyclic carbonate from CO2 and epoxides.


Synthesis ◽  
2017 ◽  
Vol 50 (03) ◽  
pp. 593-598
Author(s):  
José Morales-Serna ◽  
Bao Nguyen ◽  
Eréndira García-Ríos ◽  
Rubén Gaviño ◽  
Jorge Cárdenas ◽  
...  

The direct glycosylation of ceramides in supercritical carbon dioxide (scCO2) successfully proceeded to produce β-glycolipids in high yield and with full stereoselectivity. The reaction is promoted by montmorillonite modified with a superacid (CF3SO3H). The value of this protocol was demonstrated in the efficient synthesis of isoglobotrihexosylceramide (iGB3).


2020 ◽  
Vol 32 (4) ◽  
pp. 771-775
Author(s):  
Raiedhah A. Alsaiari

Cyclic carbonate compounds are valuable for a range of applications and can be synthesized by a one-pot reaction involving epoxidation of olefin followed by reaction of the epoxide with CO2. This study used supported ruthenium catalysts for the epoxidation step (first step), where a combination of tetrapropylammonium bromide and zinc bromide was used for the cycloaddition of carbon dioxide. The supported ruthenium catalyst, prepared by a sol-immobilization method, allowed the effective epoxidation of 1-decene in air (using oxygen as the main oxidant) at 90 ºC in the presence of a catalytic quantity of radical initiator. This approach was applied to the one-pot multi-step oxidative carboxylation of 1-decene in the presence of 1 % Ru/support-Pr4NBr/ZnBr2 catalyst


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