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• W2071737862 startingPage "3863" @default.
• W2071737862 abstract "Heavily substituted cyclopropane esters were prepared in high yields, complete diastereoselection and high (up to 96%) enantioselectivity. The reaction described herein entailed reacting 4-nitro-5-styrylisoxazoles, a class of cinnamate synthetic equivalent, with 2-bromomalonate esters under the catalysis of 5 mol% of a Cincona derived phase-transfer catalyst. The reaction allowed multi-gram preparation of desired products." @default.
• W2071737862 created "2016-06-24" @default.
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• W2071737862 date "2012-01-01" @default.
• W2071737862 modified "2023-10-18" @default.
• W2071737862 title "Phase transfer catalyzed enantioselective cyclopropanation of 4-nitro-5-styrylisoxazoles" @default.
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• W2071737862 doi "https://doi.org/10.1039/c2cc30401e" @default.
• W2071737862 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22407508" @default.
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