FeCl<sub>3</sub>-catalyzed regioselective ring-opening of aryl oxirane with 4-hydroxycoumarin for the synthesis of furo[3,2-<i>c</i>]coumarins-Reference-Cited by-同舟云学术

FeCl₃-catalyzed regioselective ring-opening of aryl oxirane with 4-hydroxycoumarin for the synthesis of furo[3,2-c]coumarins

Published:2024 Issue:1 Volume:22 Page:95-105
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Faraz Simra¹,Ali Ahmad¹,Taleb Khan Abu¹^ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati-781039, India

Abstract

The regioselective ring-opening of aryl oxiranes was investigated with various 4-hydroxycoumarins in dimethyl sulfoxide in the presence of 20 mol% FeCl3 as a catalyst at 110 °C.

Funder

CouncilofScientific and Industrial Research, India

University Grants Commission

Department of Science and Technology, Ministry of Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D3OB01721D

Reference34 articles.

1. Dicoumarol: from chemistry to antitumor benefits

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3. Recent advances in 4-hydroxycoumarin chemistry. Part 1: Synthesis and reactions

4. 4-Hydroxycoumarins. Synthesis of the metabolites and some other derivatives of warfarin

5. Current developments of coumarin-based anti-cancer agents in medicinal chemistry

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