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- W2171101768 abstract "Propargylic difluorides 1 were used as starting substrates in a combination of cross-enyne metathesis and Diels–Alder reactions. Thus, the reaction of 1 with ethylene in the presence of 2 nd generation Hoveyda–Grubbs catalyst generates a diene moiety which in situ reacts with a wide variety of dienophiles giving rise to a small family of new fluorinated carbo- and heterocyclic derivatives in moderate to good yields. This is a complementary protocol to the one previously described by our research group, which involved the use of 1,7-octadiene as an internal source of ethylene." @default.
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- W2171101768 date "2013-11-28" @default.
- W2171101768 modified "2023-10-09" @default.
- W2171101768 title "One-pot cross-enyne metathesis (CEYM)–Diels–Alder reaction of <i>gem</i>-difluoropropargylic alkynes" @default.
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- W2171101768 doi "https://doi.org/10.3762/bjoc.9.305" @default.
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