Organophotoredox-Catalyzed Formation of Alkyl–Aryl and −Alkyl C–S/Se Bonds from Coupling of Redox-Active Esters with Thio/Selenosulfonates
| Autor: | Yueteng Zhang, Wei Wang, Peng Ji, Xiang Meng, Yue Dong, Changqing Wang |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
chemistry.chemical_classification
010405 organic chemistry Aryl Organic Chemistry Thio Substrate (chemistry) 010402 general chemistry 01 natural sciences Biochemistry Medicinal chemistry Article 0104 chemical sciences Catalysis chemistry.chemical_compound chemistry Functional group Redox active Physical and Theoretical Chemistry Alkyl |
| Zdroj: | Org Lett |
| ISSN: | 1523-7052 1523-7060 |
| Popis: | A mild, organophotoredox synthetic protocol for forming C(sp3) -S/Se bond by reacting widespread redox-active esters with thio/selenosulfonates has been developed. The power of the synthetic manifold is fueled by an unprecedented broad substrate scope and wide functional group tolerance. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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