Thioamination of alkenes with hypervalent iodine reagents

Mizar, Pushpak, Niebuhr, Rebecca, Hutchings, Matthew, Farooq, Umar and Wirth, Thomas ORCID: https://orcid.org/0000-0002-8990-0667 2016. Thioamination of alkenes with hypervalent iodine reagents. Chemistry - a European Journal 22 (5) , pp. 1614-1617. 10.1002/chem.201504636

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Abstract

An efficient thioamination of alkenes mediated by iodine(III) reagents is described. The use of different sulfur nucleophiles allows the flexible synthesis of 1,2-aminothiols from alkenes. By employing chiral iodine(III) reagents, a stereoselective version of the thioamination protocol has also been developed.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Chemistry
Subjects:	Q Science > QD Chemistry
Publisher:	WileyBlackwell
ISSN:	0947-6539
Date of First Compliant Deposit:	30 March 2016
Last Modified:	16 Feb 2024 07:27
URI:	https://orca.cardiff.ac.uk/id/eprint/84933

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