Syntheses of 1,2,3-functionalized naphthols and phenols by decarboxylative cycloaddition/aromatization reactions of α-oxygenated lactones with allenoates or electron-deficient alkynes

Organic Chemistry Frontiers 2026 Open access

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Authors: Mohammad Sadeq Mousavi, António Massa, Mario Waser
DOI: 10.1039/d5qo01582k
Cited by: 1
References: 32

Abstract

Cycloadditions between hydroxypyrones or isochroman-3,4-diones and allenoates or butynoates allow for the direct synthesis of various 1,2,3-substituted phenols and naphthols.

Fields of Study & Subjects

Catalytic Alkyne Reactions Catalytic C–H Functionalization Methods Oxidative Organic Chemistry Reactions

Publication details

Journal / source
Organic Chemistry Frontiers
Publisher
Royal Society of Chemistry (RSC)
Volume
13
Issue
5
Pages
1573–1577
Publication date
1 January 2026
Language
EN