Sulfur stereogenic centers in transition-metal-catalyzed asymmetric C-H functionalization: generation and utilization

Transition-metal-catalyzed enantioselective C-H functionalization has emerged as a powerful tool for the synthesis of enantioenriched compounds in chemical and pharmaceutical industries. Sulfur-based functionalities are ubiquitous in many of the biologically active compounds, medicinal agents, funct...

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Published inChemical science (Cambridge) Vol. 12; no. 33; pp. 1972 - 1984
Main Authors Liu, Wentan, Ke, Jie, He, Chuan
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 25.08.2021
The Royal Society of Chemistry
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Summary:Transition-metal-catalyzed enantioselective C-H functionalization has emerged as a powerful tool for the synthesis of enantioenriched compounds in chemical and pharmaceutical industries. Sulfur-based functionalities are ubiquitous in many of the biologically active compounds, medicinal agents, functional materials, chiral auxiliaries and ligands. This perspective highlights recent advances in sulfur functional group enabled transition-metal-catalyzed enantioselective C-H functionalization for the construction of sulfur stereogenic centers, as well as the utilization of chiral sulfoxides to realize stereoselective C-H functionalization. This perspective highlights sulfur functional groups enabled enantioselective C-H functionalization for the construction of sulfur stereogenic centers, and the utilization of chiral sulfoxide to realize stereoselective C-H functionalization.
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ISSN:2041-6520
2041-6539
DOI:10.1039/d1sc02614c