Abstract
NpP2S4 1 (Np = C10H6, naphthalene-1,8-diyl) reacts with carbonyl groups to give thiocarbonyls whilst refluxing 1 in methanol results in cleavage of one of the P-S-P bridges and formation of the new heterocycle 3 which contains a C3P2S ring with the phosphorus atoms asymmetrically substituted by methoxy and thiomethoxy groups.
| Original language | English |
|---|---|
| Pages (from-to) | 116-117 |
| Number of pages | 2 |
| Journal | Journal of the Chemical Society, Chemical Communications |
| Issue number | 2 |
| Publication status | Published - 15 Jan 1991 |
Fingerprint
Dive into the research topics of 'REACTIONS OF 1,3-EPITHIONAPHTHO[1,8-CD][1,2-LAMBDA-5,6-LAMBDA-5]THIADIPHOSPHININE-1,3-DITHIONE - THE PREPARATION AND X-RAY STRUCTURE OF NPP(S)(SME)SP(S)(OME), THE 1ST C3P2S RING'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver