Diversified access to di- and trisubstituted allenes via nickel-catalysed reactions of 1,3-enynes with alkyl N -hydroxyphthalimide esters.
Hong LiuWan LeiYan LiYewen FangPublished in: Chemical communications (Cambridge, England) (2023)
Herein, a new nickel-catalysed protocol for the preparation of di- and trisubstituted allenes has been successfully developed via the reactions of 1,3-enynes with alkyl N -hydroxyphthalimide esters. The new method based on a reductive radical-polar crossover (RPC) process features broad substrate scope, wide functional group tolerance, and a simple catalyst system. The late-stage allenylation of drugs has also been illustrated.
Keyphrases
- ionic liquid
- reduced graphene oxide
- metal organic framework
- biofilm formation
- room temperature
- oxide nanoparticles
- visible light
- carbon nanotubes
- randomized controlled trial
- open label
- double blind
- pseudomonas aeruginosa
- molecularly imprinted
- staphylococcus aureus
- placebo controlled
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- amino acid
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- drug induced
- mass spectrometry