Existing methods for C–H activation depend on pre-installed directing groups, the removal of which poses a practical limitation on the use of these reactions in synthesis. Now, a remote-selective C−H alkylation reaction of arenes using an in situ generated spiropalladacycle has been shown to furnish benzofurans and indoles without the need for a directing group.
- Juntao Ye
- Zhihao Shi
- Mark Lautens