Abstract
A one-pot cascade reaction for the synthesis of 2-BMIDA 6,5-bicyclic heterocycles has been developed using Cu(I)/Pd(0)/Cu(II) catalysis. 2-Iodoanilines and phenols undergo a Cu(I)/Pd(0)-catalyzed Sonogashira reaction with ethynyl BMIDA followed by in situ Cu(II)-catalyzed 5-endo-dig cyclization to generate heterocyclic scaffolds with a BMIDA functional group in the 2-position. The method provides efficient access to borylated indoles, benzofurans, and aza-derivatives, which can be difficult to access through alternative methods.
Original language | English |
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Pages (from-to) | 8703-8706 |
Number of pages | 4 |
Journal | Chemical Communications |
Volume | 52 |
Issue number | 56 |
Early online date | 16 Jun 2016 |
DOIs | |
Publication status | Published - 18 Jul 2016 |
Keywords
- One-pot cascade reaction
- Sonogashira
- Heterocyclic scaffolds
- Borylated indoles
- Benzofurans
- Aza-derivatives
- BMIDA functional group