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• W4252636179 endingPage "2407" @default.
• W4252636179 startingPage "2404" @default.
• W4252636179 abstract "Abstract Readily available alkenylphenols react with allenes under rhodium catalysis to provide valuable 2,2‐disubstituted 2H‐chromenes. The whole process, which involves the cleavage of one CH bond of the alkenyl moiety and the participation of the allene as a one‐carbon cycloaddition partner, can be considered a simple, versatile, and atom‐economical (5+1) heteroannulation. The reaction tolerates a broad range of substituents both in the alkenylphenol and in the allene, and most probably proceeds through a mechanism involving a rhodium‐catalyzed CC coupling followed by two sequential pericyclic processes." @default.
• W4252636179 created "2022-05-12" @default.
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• W4252636179 date "2015-01-07" @default.
• W4252636179 modified "2023-10-18" @default.
• W4252636179 title "Rhodium‐Catalyzed (5+1) Annulations Between 2‐Alkenylphenols and Allenes: A Practical Entry to 2,2‐Disubstituted 2<i>H</i>‐Chromenes" @default.
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• W4252636179 doi "https://doi.org/10.1002/ange.201410350" @default.
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