摘要
Direct functionalization of native (N–H) indoles via C–H activation remains a challenge. Herein, we report a salicylaldehyde-promoted cobalt-catalyzed selective C2–H Heck reaction of native (N–H) indoles with both active and unactivated olefins in the presence of free N–H bonds. A series of structurally diverse C2-alkenylated native (N–H) indoles including natural product and drug derivatives were prepared directly and effectively without additional preprotection and deprotection procedures.
危险品化学品经营许可证(带存储)