scholarly journals AgI /TMG-Promoted Cascade Reaction of Propargyl Alcohols, Carbon Dioxide, and 2-Aminoethanols to 2-Oxazolidinones

ChemPhysChem ◽  
2017 ◽  
Vol 18 (22) ◽  
pp. 3182-3188 ◽  
Author(s):  
Xue-Dong Li ◽  
Qing-Wen Song ◽  
Xian-Dong Lang ◽  
Yao Chang ◽  
Liang-Nian He
2011 ◽  
Vol 353 (1) ◽  
pp. 133-146 ◽  
Author(s):  
Nicola Della Ca' ◽  
Bartolo Gabriele ◽  
Giuseppe Ruffolo ◽  
Lucia Veltri ◽  
Tito Zanetta ◽  
...  

2019 ◽  
Vol 6 (14) ◽  
pp. 2420-2429 ◽  
Author(s):  
Yao-Liang Sun ◽  
Yin Wei ◽  
Min Shi

Phosphine-catalyzed fixation of CO2 with γ-hydroxyl alkynone under ambient temperature and pressure was achieved and the first example of chiral phosphine catalyzed kinetic resolution of propargyl alcohols via carbon dioxide fixation was demonstrated.


2009 ◽  
Vol 11 (12) ◽  
pp. 2615-2618 ◽  
Author(s):  
Shaoyin Wang ◽  
Yuanxun Zhu ◽  
Yanguang Wang ◽  
Ping Lu

Author(s):  
Shu-Mei Xia ◽  
Yu Song ◽  
Xue-Dong Li ◽  
Hong-Ru Li ◽  
Liang-Nian He

To circumvent the thermodynamic limitation of the synthesis of oxazolidinones starting from 2-aminoethanols and CO2 and realize incorporation CO2 under atmospheric pressure, a protic ionic liquid-facilitated three-component reaction of propargyl alcohols, CO2 and 2-aminoethanols was developed to produce 2-oxazolidinones along with equal amount of α-hydroxyl ketones. The ionic liquid structure, reaction temperature and reaction time were in detail investigated. And 15 mol% [TBDH][TFE] (1,5,7-triazabicylo[4.4.0]dec-5-ene trifluoroethanol) was found to be able to synergistically activate the substrate and CO2, thus catalyzing this cascade reaction under atmospheric CO2 pressure. By employing this task-specific ionic liquid as sustainable catalyst, 2-aminoethanols with different substituents were successfully transformed to 2-oxazolidinones with moderate to excellent yield after 12 h at 80 oC. This three-component reaction running under atmospheric pressure proves to be a clever detour to avoid the thermodynamic issue in the synthesis of 2-oxazolidinones starting from 2-aminoethanols and CO2.


2015 ◽  
Vol 21 (9) ◽  
pp. 3585-3588 ◽  
Author(s):  
Nan Li ◽  
Tian-Yi Wang ◽  
Liu-Zhu Gong ◽  
Liming Zhang

ChemInform ◽  
2008 ◽  
Vol 39 (9) ◽  
Author(s):  
Yudai Sugawara ◽  
Wataru Yamada ◽  
Shunsuke Yoshida ◽  
Taketo Ikeno ◽  
Tohru Yamada

RSC Advances ◽  
2016 ◽  
Vol 6 (68) ◽  
pp. 63855-63858 ◽  
Author(s):  
Fu-song Wu ◽  
Wei Tong ◽  
Ying Liang ◽  
Heng-shan Wang ◽  
Qing-hu Teng ◽  
...  

We have developed a mild, robust, and multicomponent cascade reaction for the synthesis of triazolo-fused dihydrooxazinones from terminal alkynes, unactivated primary alkyl bromides, carbon dioxide and sodium azide.


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