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- W2952078322 abstract "An asymmetric tandem Michael addition–lactonization between ortho-nitrovinylphenols and azalactones was investigated for constructing 3,4-dihydrocoumarin backbones with a quaternary amino acid moiety. Under the catalysis of the chiral squaramide derived from L-tert-leucine, a wide range of substituted (E)-2-(2-nitrovinyl)phenols and azalactones were well tolerated in this tandem reaction to provide the corresponding biologically significant 3,4-dihydrocoumarin derivatives in excellent yields with high levels of diastereo- and enantioselectivity." @default.
- W2952078322 created "2019-06-27" @default.
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- W2952078322 date "2016-05-01" @default.
- W2952078322 modified "2023-09-23" @default.
- W2952078322 title "ChemInform Abstract: Stereocontrolled Construction of 3,4-Dihydrocoumarin Scaffolds with a Quaternary Amino Acid Moiety via Chiral Squaramide-Catalyzed Cascade Michael Addition/Lactonization Reaction." @default.
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- W2952078322 doi "https://doi.org/10.1002/chin.201623162" @default.
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