Gao Pan-Pan, Yan Dong-Mei, Bi Ming-Hang, Jiang Min, Xiao Wen-Jing, Chen Jia-Rong
CCNU-uOttawa Joint Research Centre, Hubei International Scientific and Technological Cooperation Base of Pesticide and Green Synthesis, Key Laboratory of Pesticides & Chemical Biology Ministry of Education, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei, 430079, P. R. China.
College of Materials, Chemistry and Chemical Engineering, Hangzhou Normal University, 2318 Yuhangtang Road, Hangzhou, 310036, P. R. China.
Chemistry. 2021 Oct 13;27(57):14195-14201. doi: 10.1002/chem.202102671. Epub 2021 Sep 16.
A visible-light-driven and room temperature photo-Wolff-Kischner reaction of sulfur ylides and N-tosylhydrazones has been developed for the first time to provide modular access to alkene synthesis. The high functional group tolerance and broad substrate scope were demonstrated by more than 60 examples. Both E- and Z-olefinic stereochemistry in the products could be controlled with excellent stereoselectivity. A series of mechanistic studies support that the reaction should proceed through a radical-carbanion crossover pathway, specifically involving addition of photo-generated sulfur ylide radical cations to N-tosylhydrazones to form carbanions and subsequent Wolff-Kischner process.
首次开发了一种可见光驱动的硫叶立德与N-甲苯磺酰腙的室温光Wolff-Kischner反应,为烯烃合成提供了模块化途径。60多个实例证明了该反应具有高官能团耐受性和广泛的底物范围。产物中的E-和Z-烯烃立体化学均可通过出色的立体选择性进行控制。一系列机理研究支持该反应应通过自由基-碳负离子交叉途径进行,具体涉及光生硫叶立德自由基阳离子加成到N-甲苯磺酰腙上形成碳负离子,随后进行Wolff-Kischner反应。