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• W3092821818 abstract "The bicyclic tetrahydro-1,2-oxazine subunit of gliovirin is synthesized through a diastereoselective copper-catalyzed cyclization of an N-hydroxyamino ester. Oxidative elaboration to the fully functionalized bicycle was achieved through a series of mild transformations. Central to this approach was the development of the first catalytic, enantioselective propargylation of an oxime to furnish a key N-hydroyxamino ester intermediate." @default.
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• W3092821818 date "2020-01-01" @default.
• W3092821818 modified "2023-10-01" @default.
• W3092821818 title "A copper-catalyzed asymmetric oxime propargylation enables the synthesis of the gliovirin tetrahydro-1,2-oxazine core" @default.
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• W3092821818 doi "https://doi.org/10.1039/d0sc04802j" @default.
• W3092821818 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8162951" @default.
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