Abstract
The first dicyclic fused thiadiazaphosphorin derivatives, namely, [1,3,4]thiadiazolo[3,2-c]-1,2,3-trihydro-[1,3,5,2]thiadiazaphosphorins (3 and 4), were synthesized by intermolecular cyclocondensation of [1,3,4]thiadiazole-2-yl-dithiocarbamic acid (1) or -dithioperoxycarbamic acid (2) with tri(dialkylamino)phosphine. 5-methyl[1,3,4]thiadiazolo[3,2-c]-2-dialkylamino-6-thiono-1,2,3-trihydro-[1,3,5, 2]thiadiazaphosphorin (3) was easily oxided into the 5-methyl [1,3,4]thiadiazolo[3,2-c]-2-dialkylamino-6-thiono-2-oxo-1,2,3-trihydro-[1,3,5,2] thiadiazaphosphorin (4) and 5-methyl-[1,3,4]thiadiazolo[3,2-c]-2-dialkylamino-6-thiono-1,2-dioxo-1,2,3- trihydro-[1,3,5,2]thiadiazaphosphorin (5).
| Original language | English |
|---|---|
| Pages (from-to) | 299-305 |
| Number of pages | 7 |
| Journal | Phosphorus, Sulfur and Silicon and the Related Elements |
| Volume | 122 |
| DOIs | |
| State | Published - 1997 |
| Externally published | Yes |
Keywords
- Cyclocondensation
- Tris(dialkylamino)phosphine
- [1;3;4]Thiadiazolo[3;2-c][1;3;5;2]thiadiazaphosphorin
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