A silver-mediated reaction between 2-ethynyl-3-(1-hydroxyprop-2-yn-1-yl)phenols or 2-ethynyl-3-(1-hydroxyprop-2-yn-1-yl)anilines and methylene isocyanides has been developed. A sequential 5-- cyclization and [3 + 2] cycloaddition process is proposed. This synthetic strategy is atom- and step-efficient and applicable to a broad scope of substrates, allowing the synthesis of valuable substituted benzofuran- and indole-pyrroles in moderate to high yields.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.joc.9b00528 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!