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- W2000373567 abstract "Abstract While 8′-trifluoromethyl ABA ( 2a ) was known to be one of the most active and stable analogs tested in assays for ABA-like activity, a thorough evaluation of its biological properties was limited by compound availability. The current synthesis, which includes the preparation of a previously unknown key intermediate 2-methyl-2-trifluoromethyl-1,4-cyclohexanedione-mono ethylene ketal ( 18 ), has been accomplished in 14 steps and 3% yield. The key fluorinated ketal intermediate 18 was prepared in six steps and 20% yield." @default.
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- W2000373567 date "1999-08-01" @default.
- W2000373567 modified "2023-09-30" @default.
- W2000373567 title "Total synthesis of (±)-8′-trifluoromethyl abscisic acid" @default.
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- W2000373567 doi "https://doi.org/10.1016/s0040-4039(99)01206-x" @default.
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