Abstract
A synthetic route into cis- and trans- isomers of [OsCl2(chiral-at- phosphorus bidentate phosphine)2] is presented. The choice of the cis- or trans- isomer of the precursor complex [OsCl2(DMSO)4] (DMSO=dimethylsulfoxide) permits selective preparation of either cis-or trans- isomers of the diphosphine complex. A structural study confirms the retention of both, stereochemistry at the metal and configuration at phosphorus in proceeding from the dimethylsulfoxide complex to form trans- [OsCl2{(R,R)-1,2-phenylenebis(methylphenylphosphine)}2].
| Original language | English |
|---|---|
| Pages (from-to) | 3579-3583 |
| Number of pages | 5 |
| Journal | Tetrahedron Asymmetry |
| Volume | 8 |
| Issue number | 21 |
| DOIs | |
| Publication status | Published - 13 Nov 1997 |
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