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- W2015653645 abstract "As part of an ongoing study of the chemistry of macrocyclic compounds 14-membered macrocyclic ethers with a variety of methyl substitution patterns were synthesized. The preparation of these macrocyclic ethers involved either the Baeyer-Villiger ring expansion of a cyclic ketone or the macrolactonization of a hydroxy acid to give a lactone. The lactone carbonyl was removed either by conversion to an intermediate thionolactone obtained by reaction with Lawesson's reagent and reduction or by direct reduction using a boron trifluoride etherate mediated sodium borohydride reaction." @default.
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- W2015653645 date "1999-11-01" @default.
- W2015653645 modified "2023-10-17" @default.
- W2015653645 title "The synthesis of 14-membered macrocyclic ethers" @default.
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- W2015653645 doi "https://doi.org/10.1016/s0040-4020(99)00846-7" @default.
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