A novel visible light mediated radical cyclization of enol lactones: a concise method for fluorinated polycyclic lactone scaffolds
A novel visible light mediated cyclization of enol lactones with difluoroacyl arenes via a free radical tandem difluoroalkylation and C–C coupling of butenolides is presented. This strategy provides a facile approach to potential biological fluorinated γ-butyrolactones with excellent diastereoselectivity.
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2016 ◽
Vol 49
(10)
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pp. 2295-2306
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Keyword(s):
Gelsemine Support Studies: Observation of an Unusual Free Radical Cyclization-Fragmentation Sequence
1995 ◽
Vol 42
(6)
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pp. 873-875
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