Sustainable Catalyst-free N-Formylation using CO2 as a Carbon Source

被引:5
作者
Li, Zhengyi [1 ]
Yang, Song [1 ]
Li, Hu [1 ]
机构
[1] Guizhou Univ, State Key Lab Breeding Base Green Pesticide & Agr, State Local Joint Lab Comprehens Utilizat Biomass, Key Lab Green Pesticide & Agr Bioengn,Ctr RD Fine, Guiyang 550025, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon dioxide; sustainable chemistry; N-formylation; amines; catalyst-free reaction; reaction mechanism; FRUSTRATED LEWIS PAIRS; BIO-IONIC LIQUIDS; HETEROCYCLIC CARBENE; ROOM-TEMPERATURE; TERMINAL ALKYNES; AMINES; REDUCTION; METHYLATION; ACTIVATION; FORMAMIDES;
D O I
10.2174/1570179418666211022160149
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The development of new sustainable catalytic conversion methods of carbon dioxide (CO2) is of great interest in the synthesis of valuable chemicals. N-formylation of CO2 with amine nucleophiles as substrates has been studied in depth. The key to benign formylation is to select a suitable reducing agent to activate CO2. This paper showcases the activation modes of CO2 and the construction strategies of sustainable and catalyst-free N-formylation systems. The research progress of catalyst-free N-formylation of amines and CO2 is reviewed. There are two broad prominent categories, namely reductive amidation of CO2 facilitated by organic solvents and ionic liquids in the presence of hydrosilane. Attention is also paid to discussing the involved reaction mechanism with practical applications and identifying the remaining challenges in this field.
引用
收藏
页码:187 / 196
页数:10
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