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Versatile and chemoselective transformation of aliphatic and aromatic secondary amides to nitriles
Hui Geng ; Pei-Qiang Huang ; Huang PQ(黄培强)
2015-06-10
关键词Synthetic methods Secondary amides Nitriles One-pot reaction Chemoselectivity
英文摘要通讯作者地址: Huang, PQ; Triflic anhydride in combination with 2-fluoropyridine effectively dehydrates secondary amides to afford nitriles under mild reaction conditions. The reaction is general in scope and compatible with the use of aliphatic, alpha,beta-unsaturated, aromatic, and heteroaromatic amides bearing either secondary, tertiary, or benzylic N-alkyl groups. The reaction also shows good to excellent chemoselectivity for the secondary amide and tolerates several labile functional groups.; Natural Science Foundation of China (NSFC) 21332007 Program for Changjiang Scholars and Innovative Research Team in University of the Ministry of Education of China
语种英语
出版者PERGAMON-ELSEVIER SCIENCE LTD
内容类型期刊论文
源URL[http://dspace.xmu.edu.cn/handle/2288/85022]  
专题化学化工-已发表论文
推荐引用方式
GB/T 7714
Hui Geng,Pei-Qiang Huang,Huang PQ. Versatile and chemoselective transformation of aliphatic and aromatic secondary amides to nitriles[J],2015.
APA Hui Geng,Pei-Qiang Huang,&黄培强.(2015).Versatile and chemoselective transformation of aliphatic and aromatic secondary amides to nitriles..
MLA Hui Geng,et al."Versatile and chemoselective transformation of aliphatic and aromatic secondary amides to nitriles".(2015).
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