C-O and C-C bond formation in the cyclisation of gem-(dialkoxymethyl)-1,6-dienes catalysed by tin(IV) triflimidate at room temperature |
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Authors: | Vito VeceKhadija Ben Hadj Hassen,Sylvain Antoniotti,Elisabet Duñ ach |
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Affiliation: | Institut de Chimie de Nice, UMR 7272 CNRS - Université de Nice Sophia Antipolis, Parc Valrose, 06108 Nice, France |
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Abstract: | We described herein a Sn(NTf2)4-catalysed cyclisation of gem-(dialkoxymethyl)-1,6-dienes and derivatives where cyclohexane or tetrahydrofuran rings are formed following either a 6-enexo-endo-trig process or a 5-exo-trig process, respectively, depending on substitution patterns. The latter process features an unusual dealkylative ether cyclisation, triggered by the strong Lewis acid character of the tin(IV) triflimidate catalyst. |
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Keywords: | Lewis superacids Diene cycloisomerisation Carbocycles Tetrahydrofurans |
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