A simple and practical synthesis of methyl benzo[b]furan-3-carboxylates

Ferdinand S. Melkonyan; Nikita E. Golantsov; Alexander V. Karchava

doi:10.3987/COM-08-11458

A simple and practical synthesis of methyl benzo[b]furan-3-carboxylates

Ferdinand S. Melkonyan^*, Nikita E. Golantsov, Alexander V. Karchava

^*Corresponding author for this work

Chemistry

Research output: Contribution to journal › Article › peer-review

13 Scopus citations

Abstract

A simple and practical two-step procedure for the preparation of 2-unsubstituted l-benzo[b]furan-3-carboxylic acid methyl esters is described. The procedure uses the copper-catalyzed intramolecular C-O bond formation and provides an efficient route to the title compounds in good to excellent yields.

Original language	English (US)
Pages (from-to)	2973-2980
Number of pages	8
Journal	Heterocycles
Volume	75
Issue number	12
DOIs	https://doi.org/10.3987/COM-08-11458
State	Published - Dec 1 2008

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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title = "A simple and practical synthesis of methyl benzo[b]furan-3-carboxylates",

abstract = "A simple and practical two-step procedure for the preparation of 2-unsubstituted l-benzo[b]furan-3-carboxylic acid methyl esters is described. The procedure uses the copper-catalyzed intramolecular C-O bond formation and provides an efficient route to the title compounds in good to excellent yields.",

author = "Melkonyan, {Ferdinand S.} and Golantsov, {Nikita E.} and Karchava, {Alexander V.}",

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AU - Melkonyan, Ferdinand S.

AU - Golantsov, Nikita E.

AU - Karchava, Alexander V.

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AB - A simple and practical two-step procedure for the preparation of 2-unsubstituted l-benzo[b]furan-3-carboxylic acid methyl esters is described. The procedure uses the copper-catalyzed intramolecular C-O bond formation and provides an efficient route to the title compounds in good to excellent yields.

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A simple and practical synthesis of methyl benzo[b]furan-3-carboxylates

Abstract

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