Amberlyst-15-catalyzed one-pot synthesis of 2-aryltetrahydrofurans from tetrahydrofuran

Hande Gunduz; Volkan Kumbaraci; Naciye Talinli

doi:10.1055/s-0032-1317195

Amberlyst-15-catalyzed one-pot synthesis of 2-aryltetrahydrofurans from tetrahydrofuran

Hande Gunduz, Volkan Kumbaraci, Naciye Talinli^*

^*Corresponding author for this work

Department of Chemistry

Istanbul Technical University

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

5 Citations (Scopus)

Abstract

A simple one-step route for the conversion of naphthols and phenols with tetrahydrofuran into corresponding 2-aryltetrahydrofurans using Amberlyst-15 as a catalyst is reported. This is the first example of the acid-mediated formation and rearrangement reactions of tetrahydrofuranyl ethers prepared from the tetrahydrofuran and aromatic/aliphatic hydroxy compounds.

Original language	English
Pages (from-to)	2473-2476
Number of pages	4
Journal	Synlett
Volume	23
Issue number	17
DOIs	https://doi.org/10.1055/s-0032-1317195
Publication status	Published - 2012

Keywords

2-aryltetrahydrofurans
Amberlyst-15
naphthols
rearrangement reactions
tetrahydrofuranyl ethers

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10.1055/s-0032-1317195

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abstract = "A simple one-step route for the conversion of naphthols and phenols with tetrahydrofuran into corresponding 2-aryltetrahydrofurans using Amberlyst-15 as a catalyst is reported. This is the first example of the acid-mediated formation and rearrangement reactions of tetrahydrofuranyl ethers prepared from the tetrahydrofuran and aromatic/aliphatic hydroxy compounds.",

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PY - 2012

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N2 - A simple one-step route for the conversion of naphthols and phenols with tetrahydrofuran into corresponding 2-aryltetrahydrofurans using Amberlyst-15 as a catalyst is reported. This is the first example of the acid-mediated formation and rearrangement reactions of tetrahydrofuranyl ethers prepared from the tetrahydrofuran and aromatic/aliphatic hydroxy compounds.

AB - A simple one-step route for the conversion of naphthols and phenols with tetrahydrofuran into corresponding 2-aryltetrahydrofurans using Amberlyst-15 as a catalyst is reported. This is the first example of the acid-mediated formation and rearrangement reactions of tetrahydrofuranyl ethers prepared from the tetrahydrofuran and aromatic/aliphatic hydroxy compounds.

KW - 2-aryltetrahydrofurans

KW - Amberlyst-15

KW - naphthols

KW - rearrangement reactions

KW - tetrahydrofuranyl ethers

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DO - 10.1055/s-0032-1317195

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SP - 2473

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JO - Synlett

JF - Synlett

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ER -

Amberlyst-15-catalyzed one-pot synthesis of 2-aryltetrahydrofurans from tetrahydrofuran

Abstract

Keywords

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