Abstract
Various S-methyl dithiocarbonates of tertiary and secondary alcohols are readily deoxygenated in high isolated yields by radical deoxygenation with di-n-butylphosphine oxide and various radical initiators in boiling dioxane. Primary alcohols react similarly in boiling xylenes.
| Original language | English |
|---|---|
| Pages (from-to) | 39-40 |
| Number of pages | 2 |
| Journal | Synlett |
| Issue number | 1 |
| Publication status | Published - 1998 Jan 1 |
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All Science Journal Classification (ASJC) codes
- Organic Chemistry
Cite this
Jang, D. O., Cho, D. H., & Barton, D. H. R. (1998). Radical deoxygenation of alcohols via their S-methyl dithiocarbonate derivatives with di-n-butylphosphine oxide as hydrogen atom donor. Synlett, (1), 39-40.