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Tetrahydrofuranylation of alcohols using hypervalent iodine reagents

French, Andrew N., Cole, Jonathan and Wirth, Thomas 2004. Tetrahydrofuranylation of alcohols using hypervalent iodine reagents. Synlett (13) , pp. 2291-2294. 10.1055/s-2004-832810

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Abstract

Alcohols are converted to their corresponding 2-tetrahydrofuranyl ethers using (diacetoxyiodo)benzene in THF. Reactions are carried out under reflux, or, more effectively, under microwave irradiation. Yields up to 81% are reported without the use of chlorinated solvents.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Chemistry
Subjects: Q Science > QD Chemistry
Uncontrolled Keywords: hypervalent iodine - bis-THF-ether adduct - oxidations - protecting groups - microwave
Publisher: Georg Thieme Verlag
ISSN: 0936-5214
Last Modified: 10 Oct 2017 13:14
URI: http://orca-mwe.cf.ac.uk/id/eprint/9766

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