Asymmetric Aza-Mannich Addition: Synthesis of Modified Chiral 2-(Ethylthio)-thiazolone Derivatives with Anticancer Potency
收藏Figshare2016-02-23 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Asymmetric_Aza_Mannich_Addition_Synthesis_of_Modified_Chiral_2_Ethylthio_thiazolone_Derivatives_with_Anticancer_Potency/2682169
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An easily prepared cinchona alkaloid derivative was found to be an effective organocatalyst in a direct, enantioselective aza-Mannich addition. By establishing a quaternary carbon stereocenter, a series of modified chiral 2-(ethylthio)-thiazolone derivatives have been obtained with excellent diastereo- and enantioselectivities. And these derivatives have been found to show anticancer activities against five different cancer cell lines using the MTT assay.
创建时间：
2016-02-23
