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- W1972685906 endingPage "4537" @default.
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- W1972685906 abstract "A chiral PYBOX-DIPH-Zn(II) catalyzed enantioselective Mukaiyama–Michael reaction of acyclic silyl enol ethers with 2-enoylpyridine N-oxides has been studied in external additive free conditions at ambient temperature. The methodology offers straightforward access to a variety of functionalized chiral 1,5-dicarbonyl compounds, which could easily be elaborated into synthetically viable pyrones via hydrolysis followed by cyclization. A transition state model has been proposed to explain the stereochemical outcome." @default.
- W1972685906 created "2016-06-24" @default.
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- W1972685906 date "2013-01-01" @default.
- W1972685906 modified "2023-10-09" @default.
- W1972685906 title "Enantioselective Mukaiyama–Michael with 2-enoyl pyridine N-oxides catalyzed by PYBOX-DIPH-Zn(ii)-complexes at ambient temperature" @default.
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- W1972685906 doi "https://doi.org/10.1039/c3ob40445e" @default.
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