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Research Article
Fluoro alcohol as reaction medium: One-pot synthesis of β-hydroxy sulfoxides from epoxidesPublished in Elsevier Science
2000
Volume: 41
Issue: 16
Pages: 2895 - 2898
β-Hydroxy sulfoxides were obtained in one-pot synthesis by the ring opening of oxiranes with thiols in hexafluoroisopropanol (HFIP) without any catalyst, followed by in situ oxidation under neutral conditions. The reaction is anti-selective. β-Hydroxy sulfoxides were transformed by pyrolysis in the corresponding allylic alcohols. (C) 2000 Elsevier Science Ltd.
Topics: Allylic rearrangement (55)%55% related to the paper, One-pot synthesis (52)%52% related to the paper, Ring (chemistry) (52)%52% related to the paper and Catalysis (50)%50% related to the paper
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About the journal
| Journal | Data powered by TypesetTetrahedron Letters |
|---|---|
| Publisher | Data powered by TypesetElsevier Science |
| ISSN | 0040-4039 |
| Open Access | No |
Authors (1)
Venkitasamy Kesavan- Snail-modulated microRNA 493 forms a negative feedback loop with the insulin-like growth factor 1 receptor pathway and blocks tumorigenesis
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