Abstract
Using rhodium complexes of tertiary phosphines with carbonyl groups beta to the P atom, ethene and CO react in methanol to give products involving increased chain growth (octane-3,6-dione, methyl 4-oxohexanoate) compared with PEt3 complexes and unsaturated products (methyl propenoate, penten-3-one and 1-methoxypentan-3-one from addition of methanol to penten-3-one); mechanistic studies suggest that the ligand carbonyl group prevents coordination of the keto group in the growing chain.
| Original language | English |
|---|---|
| Pages (from-to) | 47-48 |
| Number of pages | 2 |
| Journal | Chemical Communications |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 2001 |