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- W2949221343 abstract "Abstract New total syntheses of the cuparenic sesquiterpenes enokipodins A and B were accomplished. The key step involves a novel, cationic-controlled and palladium (II) improved, 5- endo cyclization of an α-aryl-δ-epoxynitrile. The cyclization occurs with unmatched regioselectivity and high stereoselectivity. The synthesis is completed in 5 steps achieving yields of 50% for enokipodin A and 55% for enokipodin B." @default.
- W2949221343 created "2019-06-27" @default.
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- W2949221343 date "2010-04-01" @default.
- W2949221343 modified "2023-10-18" @default.
- W2949221343 title "Palladium (II) catalyzed 5-endo epoxynitrile cyclizations: total syntheses of enokipodins A and B" @default.
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- W2949221343 doi "https://doi.org/10.1016/j.tetlet.2010.02.072" @default.
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