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- W2967503352 abstract "A Pd(II)-catalyzed mild and highly regioselective 6-endo cyclization/alkylation reaction of o-(alkynyl)styrenes with simple allylic alcohols has been developed. Under mild reaction conditions, the vinyl palladium species generated in situ after cyclization could insert a C–C double bond of allylic alcohol through a cross-coupling reaction and led to the formation of (alkyl)naphthalenes. This cascade cross-coupling reaction represents a direct and atom economic method for the construction of functionalized naphthalene derivatives in moderate to good yields." @default.
- W2967503352 created "2019-08-22" @default.
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- W2967503352 date "2019-08-15" @default.
- W2967503352 modified "2023-10-17" @default.
- W2967503352 title "Palladium-Catalyzed Cycloaromatization/Alkylation of <i>o</i>-(Alkynyl)styrenes" @default.
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- W2967503352 doi "https://doi.org/10.1021/acs.joc.9b01630" @default.
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