Thioamination of Alkenes with Hypervalent Iodine Reagents

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.

• Publication year

  2016

• Venue

  Chemistry

• Publication date

  2016-01-01

• Fields of study

  Medicine, Chemistry

• Identifiers
  DOI 10.1002/chem.201504636PMID 26660291PMCID 4725223
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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