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Synthesis of π‐Extended Carbazoles via One‐Pot C—C Coupling and Chlorination Promoted by FeCl3
Chinese Journal of Chemistry ( IF 5.4 ) Pub Date : 2020-06-08 , DOI: 10.1002/cjoc.202000230
Yang Qian 1, 2 , Jia Shang 2 , Zhen‐Hua Lyu 2 , Xin Huang 2 , Ai‐jiao Guan 3 , Li‐Jin Xu 1 , Han‐Yuan Gong 2
Affiliation  

A facile synthesis, functionalization, and emission property of N‐doped carbon‐rich halogenated compound 3,6,12,15‐tetrachloro‐9‐phenyl‐9H‐tetrabenzo[a,c,g,i]carbazole (ClCbz) was reported. Cost‐effective FeCl3 catalyst serves to break eight C—H bonds of 1,2,3,4,5‐pentaphenylpyrrole (1) and subsequently construct two C—C and four C—Cl bonds in one pot with a high yield of up to 75%.

中文翻译:

通过FeCl3促进的一锅式C-C偶联和氯化合成π扩展咔唑

据报道,N掺杂的富碳卤代化合物3,6,12,15-四氯-9-苯基-9H-四苯并[a,c,g,i]咔唑(ClCbz)的合成,功能化和发射性质。具有成本效益的FeCl 3催化剂用于破坏1,2,3,4,5-五苯基吡咯(1)的8个C-H键,然后在一个罐中以高收率构建2个C-C和4个C-Cl键。高达75%。
更新日期:2020-06-08
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