Organic and pharmaceutical synthesis have traditionally relied on the stepwise transformation ofactivated functional groups to synthesize cyclic molecules.The design of valuable heterocyclic compounds,for instance,has...Organic and pharmaceutical synthesis have traditionally relied on the stepwise transformation ofactivated functional groups to synthesize cyclic molecules.The design of valuable heterocyclic compounds,for instance,has depended on multi-step routes such as polar or radical cyclization,cycloadditions,and the manipulation of various functional groups to achieve ring formation or connection[1,2].展开更多
基金supported by the MSIT(2022R1F1A106268,RS-2023-00213491,RS-2023-00219859,RS-2024-00405261,RS-2024-00409589,RS-2025-25460522,and RS-2025-00642970)Republic of Korea,the InnoCORE program of the Ministry of Science and ICT of Korea(N10250153 and 1.250022.01)the Creative Research Program and KAIST Cross-Generation Collaborative Lab Project.
文摘Organic and pharmaceutical synthesis have traditionally relied on the stepwise transformation ofactivated functional groups to synthesize cyclic molecules.The design of valuable heterocyclic compounds,for instance,has depended on multi-step routes such as polar or radical cyclization,cycloadditions,and the manipulation of various functional groups to achieve ring formation or connection[1,2].
