Issue 45, 2024

Silver-catalyzed regioselective synthesis of pyrano heterocycles: a versatile route to samoquasine A derivatives

Abstract

This study introduces a silver-catalyzed method for the efficient and regioselective synthesis of pyrano heterocycles, utilizing readily available alcohols and water as nucleophiles. The method demonstrates high efficiency, delivering excellent yields and selectivity, and is scalable to gram quantities while maintaining broad functional group tolerance. Notably, the synthesized pyrano[3,4-c]quinolines were successfully transformed into diverse samoquasine A derivatives, underscoring the method's applicability in natural product synthesis. This work represents a significant advancement in pyrano heterocycle synthesis, offering a practical route to valuable compounds with potential applications in pharmaceutical and chemical research.

Graphical abstract: Silver-catalyzed regioselective synthesis of pyrano heterocycles: a versatile route to samoquasine A derivatives

Supplementary files

Article information

Article type
Paper
Submitted
04 Sep 2024
Accepted
08 Oct 2024
First published
11 Oct 2024

Org. Biomol. Chem., 2024,22, 8898-8903

Silver-catalyzed regioselective synthesis of pyrano heterocycles: a versatile route to samoquasine A derivatives

K. Chahal, R. Badhavath, S. K. Matharu, A. Vinod, D. Vani, V. R. Potluri, B. Sridhar and K. R. Reddy, Org. Biomol. Chem., 2024, 22, 8898 DOI: 10.1039/D4OB01446D

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