Abstract
A highly efficient CoI 2 /o-phenanthroline catalyzed cycloaddition reaction of diynes bearing TBS protected propargylic alcohol fragments with nitriles has been developed. This methodology offers regioselective access, with good functional group tolerance, to various indeno[2,1-c]pyridine derivatives in moderate to excellent yields. It was found that o-phenanthroline as a bidentate nitrogen ligand showed high efficacy in this cycloaddition reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 8761-8768 |
| Number of pages | 8 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 16 |
| Issue number | 45 |
| DOIs | |
| State | Published - 2018 |
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