Silver-Mediated Synthesis of Substituted Benzofuran- and Indole-Pyrroles via Sequential Reaction of -Alkynylaromatics with Methylene Isocyanides.

J Org Chem

School of Chemistry and Materials Science, Jiangsu Key Laboratory of Green Synthesis for Functional Materials , Jiangsu Normal University, Xuzhou , Jiangsu 221116 , China.

Published: July 2019

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.9b00528DOI Listing

Publication Analysis

Top Keywords

substituted benzofuran-
8
benzofuran- indole-pyrroles
8
methylene isocyanides
8
silver-mediated synthesis
4
synthesis substituted
4
indole-pyrroles sequential
4
sequential reaction
4
reaction -alkynylaromatics
4
-alkynylaromatics methylene
4
isocyanides silver-mediated
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!