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- W2032862014 abstract "The functionalized pyroglutamate core unit, (2R,4R)-3, which could be converted into the β-lactone/pyrrolidine or γ-lactone/pyrrolidine ring system of oxazolomycin A 1 and neooxazolomycin 2, and which possesses an exomethylene group at C3 as a scaffold for the construction of their C3 polyene segment, was synthesized by the Michael reaction of a glycine Schiff base 4 with the α,β-disubstituted acrylate 8 as the key step." @default.
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- W2032862014 date "2008-12-01" @default.
- W2032862014 modified "2023-10-17" @default.
- W2032862014 title "Efficient asymmetric synthesis of the functionalized pyroglutamate core unit common to oxazolomycin and neooxazolomycin using Michael reaction of nucleophilic glycine Schiff base with α,β-disubstituted acrylate" @default.
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- W2032862014 doi "https://doi.org/10.1016/j.tetasy.2008.11.036" @default.
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