Journal
ORGANIC LETTERS
Volume 11, Issue 18, Pages 4084-4087Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol9015578
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- NSFC [20672136, 20702060, 20832006]
- STCSM [07XD14038]
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With the catalysis of CuI/trans-N,N'-dimethylcyclohexane-1,2-diamine, a number of carboxylic acids underwent efficient intramolecular O-vinylation with vinyl bromides leading to the synthesis of the corresponding five- and six-membered enol lactones. The same catalytic system also led to the efficient cycloisomerization of alkynoic acids.
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