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- W1966598330 abstract "The milbemycin β1 analogue (38) has been prepared by a convergent route involving the Wittig condensation between phosphonium salt (28) and 5-hydroxy-5H-furan-2-one (11), followed by diene isomerization, transprotection, lactonization, and reduction; the structure of the ester intermediate (37) was established by X-ray crystallography." @default.
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- W1966598330 date "1985-01-01" @default.
- W1966598330 modified "2023-10-09" @default.
- W1966598330 title "Synthesis of a macrocyclic analogue of milbemycin β<sub>1</sub>; X-ray structure of (1RS, 4RS, 6SR, 7SR, 19RS)-(10Z, 12E, 16E)-6,16-dimethyl-9-hydroxy-7-methoxy-10-methoxycarbonyl-2-oxatricyclo[17.3.1.0<sup>4,9</sup>]tricosa-10,12,16-trien-3-one" @default.
- W1966598330 doi "https://doi.org/10.1039/c39850000755" @default.
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