4.8 Article

An approach to the core skeleton of lancifodilactone F

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ORGANIC LETTERS
卷 10, 期 6, 页码 1223-1226

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AMER CHEMICAL SOC
DOI: 10.1021/ol800111j

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Two cycloaddition reactions were utilized for the construction of the 5,6,7-tricyclic skeleton of lancifodilactone F and buxapentalactone. A [2+2] ketene cycloaddition reaction was first used to set their adjacent all-carbon quaternary centers at the 5,6-ring junction. An arene-olefin meta-photocycloaddition reaction was then used to install the 6- and 7-membered rings concurrently.

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