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- W2949556410 abstract "Cycloadduct from 3-ethynyl-5-bromo-2-pyrone undergoes facile cyclocarbopalladation reactions to provide an array of polycarbocyclic compounds with a complete control of the olefin geometry. Both organotin and boron reagents can be used as a trapping anion source. Treatment of the resulting tetracycles with NaOMe gave rise to various tetrahydrofluorenes in good to excellent isolated yields." @default.
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- W2949556410 date "2003-06-01" @default.
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- W2949556410 title "Synthesis of tetrahydrofluorenes from the cycloadduct of 3-ethynyl-5-bromo-2-pyrone via cyclocarbopalladation reactions" @default.
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- W2949556410 doi "https://doi.org/10.1016/s0040-4039(03)01032-3" @default.
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