Abstract
A number of 6-methyl-5-phenyl-2-sulfido-1,2,3,5-tetrahydro-4H[1,2]oxazolo[4′,5′: 5,6]pyrano[2,3-d][1,3,2]diazaphosphinines 4–11 were synthesized via an interaction of tetraphosphorus decasulfide and Lawesson’s reagent under different conditions with 6-amino-3-methyl-4-phenyl-4H-pyrano[3,2-d][1,2]oxazole-5-carbonitrile (3). The reaction mechanisms for these products were discussed. Structures of the newly synthesized products were established on the basis of elemental analysis and spectral data.
| Original language | English |
|---|---|
| Pages (from-to) | 472-482 |
| Number of pages | 11 |
| Journal | Journal of Sulfur Chemistry |
| Volume | 39 |
| Issue number | 5 |
| DOIs | |
| State | Published - 3 Sep 2018 |
| Externally published | Yes |
Keywords
- 1,3,2-Diazaphosphinine
- Lawesson’s reagent
- pyrano[3,2-d][1,2]oxazole
- tetraphosphorus decasulfide
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