酰腈
外观
(重定向自酰腈)
在有机化学中,
合成
[编辑]或者,它们可以通过酰基醛肟(英语:Acyl aldoxime)脱水获取:
反应
[编辑]酰腈是温和的酰化剂。[3]
参考资料
[编辑]- ^ 樂詞網--醯基氰化物. 国家教育研究院. [2023-08-11]. (原始内容存档于2023-08-11).
- ^ Liu, Bing; Wang, Yong; Chen, Ying; Wu, Qian; Zhao, Jing; Sun, Jianwei. Stereoselective Synthesis of Fully-Substituted Acrylonitriles via Formal Acylcyanation of Electron-Rich Alkynes. Organic Letters. 2018, 20 (12): 3465–3468. PMID 29873500. doi:10.1021/acs.orglett.8b01180.
- ^ 3.0 3.1 Morris, Joel. Encyclopedia of Reagents for Organic Synthesis. 2001. ISBN 0471936235. doi:10.1002/047084289X.ra026.
- ^ Demko, Zachary P.; Sharpless, K. Barry. A Click Chemistry Approach to Tetrazoles by Huisgen 1,3-Dipolar Cycloaddition: Synthesis of 5-Acyltetrazoles from Azides and Acyl Cyanides. Angewandte Chemie International Edition. 2002, 41 (12): 2113–2116. PMID 19746613. doi:10.1002/1521-3773(20020617)41:12<2113::AID-ANIE2113>3.0.CO;2-Q.