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Base-Promoted Reaction of 4-Chloro-3-vinyl Coumarins, Phenacylpyridinium Bromides, and Elemental Sulfur: A Designed Approach to Thiopyrano[4,3-<i>c</i>]chromen-5(1<i>H</i>)-ones

Behnaz Farajpour, Abdolali Alizadeh

2022The Journal of Organic Chemistry17 citationsDOI

Abstract

)-ones was developed based on a base-promoted three-component reaction between 4-chloro-3-vinyl coumarins, phenacylpyridinium bromides, and elemental sulfur. Readily available starting materials, mild conditions, chemoselectivity, operational simplicity, and synthetically useful yields are some highlighted advantages of these transformations.

Topics & Concepts

ChemoselectivitySulfurChemistryBase (topology)Organic chemistryReaction conditionsCombinatorial chemistryCatalysisMathematicsMathematical analysisSulfur-Based Synthesis TechniquesSynthesis of Organic CompoundsMulticomponent Synthesis of Heterocycles
Base-Promoted Reaction of 4-Chloro-3-vinyl Coumarins, Phenacylpyridinium Bromides, and Elemental Sulfur: A Designed Approach to Thiopyrano[4,3-<i>c</i>]chromen-5(1<i>H</i>)-ones | Litcius