Graduate School of Pharmaceutical Sciences, Tohoku University.
Chem Pharm Bull (Tokyo). 2021;69(8):707-716. doi: 10.1248/cpb.c21-00389.
This account summarizes the development of a benzyne-mediated cyclization/functionalization protocol for the versatile construction of highly substituted benzene derivatives fused with an N-heterocyclic ring such as indolines, indoles, and related nitrogen-containing heterocycles. The protocol comprises sequential reactions initiated by generating a benzyne species and subsequent cyclization via addition of magnesium amide to the benzyne, followed by trapping of the resultant magnesium compound in situ with various electrophiles. The substituent scope was expanded by conducting a transmetalation on a copper species to introduce alkyl, aryl, and alkenyl substituents. The utility of the sequential reaction was demonstrated in the synthesis of a carbazole natural product (heptaphylline), pyrrolo[4,3,2-de]quinoline alkaloids (batzellines), and pyrrolo[2,3-c]carbazole alkaloids (dictyodendrines).
本账户总结了一种苯炔介导的环化/官能化方法的发展,该方法可用于灵活构建高度取代的苯衍生物,这些苯衍生物与 N-杂环如吲哚啉、吲哚和相关含氮杂环稠合。该方案包括通过生成苯炔物种引发的顺序反应,然后通过镁酰胺与苯炔加成进行环化,随后用各种亲电试剂原位捕获所得的镁化合物。通过对铜物种进行转金属化来扩大取代基范围,引入烷基、芳基和烯基取代基。该连续反应的实用性在咔唑天然产物(heptaphylline)、吡咯并[4,3,2-de]喹啉生物碱( batzellines)和吡咯并[2,3-c]咔唑生物碱(dictyodendrines)的合成中得到了证明。