Journal
CHEMICAL COMMUNICATIONS
Volume 55, Issue 46, Pages 6539-6542Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc03023a
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- First Bank of Toyama
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Regioselective ring-opening cyclization of cyclohexane-1,3-dione-2-spirocyclopropanes with stabilized sulfonium ylides provided 2,3-trans-disubstituted 2,3,4,6,7,8-hexahydro-5H-1-benzopyran-5-ones in high yields without the formation of any isomers. The obtained product was readily converted into highly substituted chromane.
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