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- W2106570657 abstract "Six different eupomatenoids (1a–c, 1f–h) were prepared from 2,3,5-tribromobenzofuran (2) in a concise and high-yielding synthetic sequence. The overall yields vary between 29 and 60% over four to six steps. Key to the success of the syntheses is the high regioselectivity achieved in three Pd(0)- and Ni(0)-catalyzed cross-coupling reactions which were conducted consecutively. The order of substitution at the benzofuran nucleus is C-2, C-5 and C-3." @default.
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- W2106570657 date "2002-12-01" @default.
- W2106570657 modified "2023-10-18" @default.
- W2106570657 title "Synthesis of eupomatenoids by three consecutive transition metal-catalyzed cross-coupling reactions" @default.
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- W2106570657 doi "https://doi.org/10.1016/s0040-4039(02)02287-6" @default.
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