Tetrahydrofuranylation of alcohols using hypervalent iodine reagents

French, Andrew N., Cole, Jonathan and Wirth, Thomas ORCID: https://orcid.org/0000-0002-8990-0667 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:	18 Oct 2022 12:25
URI:	https://orca.cardiff.ac.uk/id/eprint/9766

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