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- W2007381041 abstract "We present here the application of Grubbs’ 2nd generation catalyst for the ring-closing metathesis of electron-deficient α,β-unsaturated amides and esters leading to the synthesis of enantiopure azepinone and oxepinone derivatives on a carbohydrate glycoside scaffold. The relative stereochemistries of the compounds obtained were corroborated by X-ray crystallography, 1H NMR or deduced based on previously reported results. These compounds are designed as precursors of new polyhydroxylated heteroannulated sugars with potential biological activity." @default.
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- W2007381041 date "2009-07-01" @default.
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- W2007381041 title "Stereoselective synthesis of seven-membered lactams and lactones on a carbohydrate scaffold using ring-closing metathesis" @default.
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- W2007381041 doi "https://doi.org/10.1016/j.tetlet.2009.03.125" @default.
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