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.
CITATION STYLE
Mizar, P., Niebuhr, R., Hutchings, M., Farooq, U., & Wirth, T. (2016). Thioamination of Alkenes with Hypervalent Iodine Reagents. Chemistry - A European Journal, 22(5), 1614–1617. https://doi.org/10.1002/chem.201504636
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