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 |
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Pages (from-to) | 47-48 |
Number of pages | 2 |
Journal | Chemical Communications |
Issue number | 1 |
DOIs | |
Publication status | Published - 2001 |