Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, People's Republic of China.
Chem Commun (Camb). 2022 Aug 18;58(67):9409-9412. doi: 10.1039/d2cc03221j.
Sulfonyl fluorides are emerging as key structural motifs in organic synthesis, medicinal chemistry, and materials science. Herein we report two efficient and complementary methods for direct decarboxylative fluorosulfonylation of carboxylic acids by the merging of copper catalysis with different -centered HAT regents. A wide range of structurally diverse sulfonyl fluorides was readily accessed from primary, secondary, and tertiary carboxylic acids in a single step under mild conditions.
磺酰氟在有机合成、药物化学和材料科学中作为关键结构基元正在兴起。在此,我们通过铜催化与不同的 C-centered HAT 试剂的结合,报告了两种用于直接脱羧磺酰氟化的高效且互补的方法。在温和条件下,从伯、仲和叔羧酸一步即可轻松获得结构多样的各种磺酰氟化物。