期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 10, 期 24, 页码 4759-4766出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ob25271f
关键词
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N-Aryl 4-methylene-2-oxazolidinones, prepared via the corresponding O-propargyl carbamates, underwent nitrile oxide cycloaddition with benzonitrile oxide to give 5-spiro isoxazoline adducts with complete regioselectivity. Steric hindrance by atropisomerism around the N-aryl bond induced facial selectivity in these cycloadditions.
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