Natural Compounds and Their Structural Analogs in Regio- and Stereoselective Synthesis of New Families of Water-Soluble 2,3-[1,3]thia- and -Selenazolo[3,2-]pyridin-4-ium Heterocycles by Annulation Reactions

Overview

Journal Molecules

Publisher MDPI

Specialty Biology

Date 2020 Jan 23

PMID 31963275

Citations 6

Authors

Vladimir A Potapov

Roman S Ishigeev

Irina V Shkurchenko

Sergey V Zinchenko

Svetlana V Amosova

Affiliations

Soon will be listed here.

Abstract

It has been found that both eugenol and isoeugenol derivatives reacted with 2-pyridinesulfenyl and 2-pyridineselenenyl halides in a regioselective mode affording products with opposite regiochemistry. Synthesis of new families of 2,3-[1,3]thia- and -selenazolo[3,2-]pyridin-4-ium heterocycles has been developed by annulation reactions of 2-pyridinechalcogenyl halides with natural compounds (eugenol, isoeugenol, methyl eugenol, methyl isoeugenol, acetyl eugenol, trans-anethole) and their structural analogs. The influence of the substrate structure and the nature of halogen on the product yields are studied. The 2-pyridinesulfenyl and 2-pyridineselenenyl chlorides are more efficient reagents compared to corresponding bromides. The obtained condensed heterocycles are novel water-soluble functionalized compounds with promising biological activity.

Citing Articles

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