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Catalytic Conversion of Carbon Dioxide through C-N Bond

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Catalytic Conversion of Carbon Dioxide through C-N Bond ( catalytic-conversion-carbon-dioxide-through-c-n-bond )

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Molecules 2019, 24, 182 35 of 41 6. Yang, Z.-Z.; He, L.-N.; Gao, J.; Liu, A.-H.; Yu, B. Carbon dioxide utilization with C–N bond formation: Carbon dioxide capture and subsequent conversion. Energy Environ. Sci. 2012, 5, 6602–6639. [CrossRef] 7. Cokoja, M.; Bruckmeier, C.; Rieger, B.; Herrmann, W.A.; Kuhn, F.E. Transformation of carbon dioxide with homogeneous transition-metal catalysts: A molecular solution to a global challenge? Angew. Chem. Int. Ed. 2011, 50, 8510–8537. [CrossRef] 8. Sakakura, T.; Choi, J.-C.; Yasuda, H. Transformation of carbon dioxide. Chem. Rev. 2007, 107, 2365–2387. [CrossRef] 9. Liu, Q.; Wu, L.; Jackstell, R.; Beller, M. Using carbon dioxide as a building block in organic synthesis. Nat. Commun. 2015, 6, 5933–5948. [CrossRef] 10. Klankermayer, J.; Wesselbaum, S.; Beydoun, K.; Leitner, W. Selective catalytic synthesis using the combination of carbon dioxide and hydrogen: Catalytic chess at the interface of energy and chemistry. Angew. Chem. Int. Ed. 2016, 55, 7296–7343. [CrossRef] 11. Song, Q.-W.; Zhou, Z.-H.; He, L.-N. Efficient, selective and sustainable catalysis of carbon dioxide. Green Chem. 2017, 19, 3707–3728. [CrossRef] 12. Song, Q.-W.; Zhao, Y.-N.; He, L.-N.; Gao, J.; Yang, Z.-Z. Synthesis of oxazolidinones/polyurethanes from aziridines and CO2. Curr. Catal. 2012, 1, 107–124. [CrossRef] 13. Liu, X.-F.; Wang, M.-Y.; He, L.-N. Heterogeneous catalysis for oxazolidinone synthesis from aziridines and CO2. Curr. Org. Chem. 2017, 21, 698–707. [CrossRef] 14. Pulla, S.; Felton, C.M.; Ramidi, P.; Gartia, Y.; Ali, N.; Nasini, U.B.; Ghosh, A. Advancements in oxazolidinone synthesis utilizing carbon dioxide as a C1 source. J. CO2 Util. 2013, 2, 49–57. [CrossRef] 15. Tamura, M.; Honda, M.; Nakagawa, Y.; Tomishige, K. Direct conversion of CO2 with diols, aminoalcohols and diamines to cyclic carbonates, cyclic carbamates and cyclic ureas using heterogeneous catalysts. J. Chem. Technol. Biotechnol. 2014, 89, 19–33. [CrossRef] 16. Wang, H.; Xin, Z.; Li, Y. Synthesis of ureas from CO2. Top Curr. Chem. 2017, 375, 1–26. 17. Song, Q.-W.; He, L.-N. Heterocyclic synthesis through C-N bond formation with carbon dioxide in chemistry beyond chlorine. In Chemistry Beyond Chlorine; Springer International Publishing: Basel, Switzerland, 2016; Chapter 16; pp. 435–453. 18. Liu, H.; Hua, R. Conversion of carbon dioxide into 2-oxazolidinones and 2(3H)-oxazolones catalyzed by 2,2′,2′′-terpyridine. Tetrahedron 2016, 72, 1200–1204. [CrossRef] 19. Arshadi, S.; Vessally, E.; Hosseinian, A.; Soleimani-amiri, S.; Edjlali, L. Three-component coupling of CO2, propargyl alcohols, and amines: An environmentally benign access to cyclic and acyclic carbamates. J. CO2 Util. 2017, 21, 108–118. [CrossRef] 20. Gu, Y.; Zhang, Q.; Duan, Z.; Zhang, J.; Zhang, S.; Deng, Y. Ionic liquid as an efficient promoting medium for fixation of carbon dioxide: A clean method for the synthesis of 5-methylene-1,3-oxazolidin-2-ones from propargylic alcohols, amines, and carbon dioxide catalyzed by Cu(I) under mild conditions. J. Org. Chem. 2005, 70, 7376–7380. [CrossRef] 21. Song, Q.-W.; Yu, B.; Li, X.-D.; Ma, R.; Diao, Z.-F.; Li, R.-G.; Li, W.; He, L.-N. Efficient chemical fixation of CO2 promoted by a bifunctional Ag2WO4/Ph3P system. Green Chem. 2014, 16, 1633–1638. [CrossRef] 22. Xu, J.; Zhao, J.; Jia, Z.; Zhang, J. Facile and mild process for chemical fixation of CO2 to 4-methylene- 1,3-oxazolidin-2-ones under solvent-free conditions. Synth. Commun. 2011, 41, 858–863. [CrossRef] 23. Jiang, H.; Zhao, J.; Wang, A. An efficient and eco-friendly process for the conversion of carbon dioxide into oxazolones and oxazolidinones under supercritical conditions. Synthesis 2008, 2008, 763–769. [CrossRef] 24. Ca, N.D.; Gabriele, B.; Ruffolo, G.; Veltri, L.; Zanetta, T.; Costa, M. Effective guanidine-catalyzed synthesis of carbonate and carbamate derivatives from propargyl alcohols in supercritical carbon dioxide. Adv. Synth. Catal. 2011, 353, 133–146. [CrossRef] 25. Zhang, Q.; Shi, F.; Gu, Y.; Yang, J.; Deng, Y. Efficient and eco-friendly process for the synthesis of N-substituted 4-methylene-2-oxazolidinones in ionic liquids. Tetrahedron Lett. 2005, 46, 5907–5911. [CrossRef] 26. Jiang, H.-F.; Zhao, J.-W. Silver-catalyzed activation of internal propargylic alcohols in supercritical carbon dioxide: Efficient and eco-friendly synthesis of 4-alkylidene-1,3-oxazolidin-2-ones. Tetrahedron Lett. 2009, 50, 60–62. [CrossRef] 27. Zhang, G.; Yang, H.; Fei, H. Unusual missing linkers in an organosulfonate-based primitive-cubic (pcu)-type metal-organic framework for CO2 capture and conversion under ambient conditions. ACS Catal. 2018, 8, 2519–2525. [CrossRef]

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