Abstract
The loss of and 1H 2H during the formation of (2—4η)-PdCl compounds from deuterio-substituted 1-acetyl-4-t-butylcyclohex-l-enes shows little stereoselectivity and is compatible with a mechanism of formation which involves an initial palladium-assisted enolisation of the enone.
Original language | English |
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Pages (from-to) | 139-141 |
Number of pages | 3 |
Journal | Journal of the Chemical Society, Chemical Communications |
Issue number | 4 |
DOIs | |
Publication status | Published - 1 Jan 1980 |