School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka, 422-8526, Japan.
Angew Chem Int Ed Engl. 2020 Aug 10;59(33):14101-14105. doi: 10.1002/anie.202005367. Epub 2020 Jun 4.
A linked dicarboxylate phase-transfer catalyst enables smooth asymmetric dearomative fluorination of 2-naphthols with Selectfluor under mild conditions to give the corresponding 1-fluoronaphthalenone derivatives in a highly enantioselective manner. This reaction, which is compatible with a range of functional groups, is the first example of catalytic asymmetric fluorination of 2-naphthols, and is expected to be useful in the synthesis of bioactive molecules.
一种链接的二羧酸酯相转移催化剂可以在温和条件下使 2-萘酚与 Selectfluor 顺利地进行不对称去芳构化氟化反应,以高对映选择性地得到相应的 1-氟萘满酮衍生物。该反应与多种官能团兼容,是首例催化不对称氟化 2-萘酚的反应,有望在生物活性分子的合成中发挥作用。