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- W2289176767 endingPage "4263" @default.
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- W2289176767 abstract "A highly enantioselective formal [3 + 2] cycloaddition reaction between 3-isothiocyanato oxindoles and alkynyl ketones is reported for the first time. An oxazoline-OH type chiral ligand derived from o-hydroxy-phenylacetic acid is employed to generate an effective magnesium catalyst in the current cyclization reaction and give serials of chiral spirooxindoles with good chemical yields and enantioselectivities." @default.
- W2289176767 created "2016-06-24" @default.
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- W2289176767 date "2015-08-20" @default.
- W2289176767 modified "2023-10-14" @default.
- W2289176767 title "Catalytic Asymmetric [3 + 2] Cyclization Reactions of 3-Isothiocyanato Oxindoles and Alkynyl Ketones Via an in Situ Generated Magnesium Catalyst" @default.
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- W2289176767 doi "https://doi.org/10.1021/acs.orglett.5b02052" @default.
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