Valorization of Carbon Dioxide into Oxazolidinones by Reaction with Aziridines
作者： Katie J. Lamb , Ian D.V. Ingram , Michael North , Mani Sengoden
DOI: 10.2174/2213346106666190321142328
关键词:
摘要: The reduction of carbon dioxide has gained much attention due to increasing environmental concerns about global warming associated with emissions from industrial effluents and public transport etc. In this regard, considerable been devoted the chemical conversion dioxide, its incorporation into synthetic organic molecules under mild “green” conditions. recent years, significant effort dedicated studying fixation aziridines afford oxazolidinones, which is an friendly atom economical process. review, we discuss efficiency different catalytic systems, by comparing analyzing each reaction parameter such as pressure, temperature, substrate scope product selectivity.
eurekaselect.com参考文章(51)
Shuai Zhang, Yu-Nong Li, Ya-Wei Zhang, Liang-Nian He, Bing Yu, Qing-Wen Song, Xian-Dong Lang, Equimolar Carbon Absorption by Potassium Phthalimide and In Situ Catalytic Conversion Under Mild Conditions Chemsuschem. ,vol. 7, pp. 1484- 1489 ,(2014) , 10.1002/CSSC.201400133
D. A. Evans, J. Bartroli, T. L. Shih, Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates Journal of the American Chemical Society. ,vol. 103, pp. 2127- 2129 ,(1981) , 10.1021/JA00398A058
Zhen-Zhen Yang, Liang-Nian He, Shi-Yong Peng, An-Hua Liu, Lewis basic ionic liquids-catalyzed synthesis of 5-aryl-2-oxazolidinones from aziridines and CO2 under solvent-free conditions Green Chemistry. ,vol. 12, pp. 1850- 1854 ,(2010) , 10.1039/C0GC00286K
Haruo Matsuda, Akira Ninagawa, Hiroshi Hasegawa, Reaction of Carbon Dioxide with 1-Phenylaziridine Catalyzed by Organo-antimony and -tin Compounds Bulletin of the Chemical Society of Japan. ,vol. 58, pp. 2717- 2718 ,(1985) , 10.1246/BCSJ.58.2717
Aaron W. Miller, SonBinh T. Nguyen, (Salen)chromium(III)/DMAP: An efficient catalyst system for the selective synthesis of 5-substituted oxazolidinones from carbon dioxide and aziridines Organic Letters. ,vol. 6, pp. 2301- 2304 ,(2004) , 10.1021/OL049689T
GEORGE P. SPERANZA, W. J. PEPPEL, Preparation of Substituted 2-Oxazolidones from 1,2-Epoxides and Isocyanates Journal of Organic Chemistry. ,vol. 23, pp. 1922- 1924 ,(1958) , 10.1021/JO01106A027
Atsushi Sudo, Yosuke Morioka, Eri Koizumi, Fumio Sanda, Takeshi Endo, Highly efficient chemical fixations of carbon dioxide and carbon disulfide by cycloaddition to aziridine under atmospheric pressure Tetrahedron Letters. ,vol. 44, pp. 7889- 7891 ,(2003) , 10.1016/J.TETLET.2003.09.011
Xiu-Zhen Lin, Zhen-Zhen Yang, Liang-Nian He, Zhong-Yong Yuan, Mesoporous zirconium phosphonates as efficient catalysts for chemical CO2 fixation Green Chemistry. ,vol. 17, pp. 795- 798 ,(2015) , 10.1039/C4GC01709A
Christopher Beattie, Michael North, Mechanistic Investigation of the Reaction of Epoxides with Heterocumulenes Catalysed by a Bimetallic Aluminium Salen Complex Chemistry - A European Journal. ,vol. 20, pp. 8182- 8188 ,(2014) , 10.1002/CHEM.201400007
Patricia Tascedda, Elisabet Duñach, Electrosynthesis of cyclic carbamates from aziridines and carbon dioxide Chemical Communications. pp. 449- 450 ,(2000) , 10.1039/A910285J