Abstract
Cyclopentenone derivatives are obtained from alkynes, allyl halides and carbon monoxide in a single synthetic operation by the use of Ni(COD) 2 with minimal formation (if any) of Ni(CO) 4. The initial formation of a π-allyl nickel complex, first intermediate in the so far postulated mechanism, is a valid pathway to the three component cycloaddition. However, care should be taken to minimize the side reactions in the process, the extension of which depends on the nature of both the alkyne and the allyl derivatives. Reliable monitoring of the components throughout the process results in good yields of the cycloadducts.
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