Abstract
In their recent report in Nature, Ritter and co-workers took advantage of a persistent sulfur-based radical cation to regioselectively install a thianthrene motif in simple or complex (hetero)arenes, and the resulting thianthrenium salts could undergo divergent late-stage transformations, offering chemists a powerful platform for introducing versatile functional groups and substituents in (hetero)arene rings.
Original language | English |
---|---|
Pages (from-to) | 1025-1027 |
Number of pages | 3 |
Journal | Chem |
Volume | 5 |
Issue number | 5 |
DOIs | |
Publication status | Published - May 9 2019 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2019
ASJC Scopus Subject Areas
- General Chemistry
- Biochemistry
- Environmental Chemistry
- General Chemical Engineering
- Biochemistry, medical
- Materials Chemistry