Biomimetic Desymmetrization of a Carboxylic Acid
收藏Figshare2018-02-05 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Biomimetic_Desymmetrization_of_a_Carboxylic_Acid/5853732
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The enantioselective desymmetrization of carboxylic acids by chiral Brønsted base catalysis is reported, leading to bridged bicyclic lactones with up to 94% ee. Crystallographic analysis of a substrate–catalyst complex suggests an origin of stereocontrol, reminiscent of functional Brønsted bases in biological settings, and enabled reaction optimization. The products contain an all-carbon quaternary stereocenter and can be derivatized to functionalized cyclopentanes.
创建时间:
2018-02-05



