Abstract
In stark contrast to phenothiazines and their prevalence for cross-dehydrogenative amination reactions, benzophenothiazine has a pronounced preference for cross-dehydrogenative C-C bond-forming reactions. Moreover, the substrate is very versatile, leading to several new classes of C-C bond-forming reactions and many new oxidative coupling product architectures, including unprecedented indole fused paddlewheel-like structures.
Cite
CITATION STYLE
Bub, C. L., Thönnißen, V., & Patureau, F. W. (2020). Benzophenothiazine and Its Cr(III)-Catalyzed Cross Dehydrogenative Couplings. Organic Letters, 22(23), 9196–9198. https://doi.org/10.1021/acs.orglett.0c03354
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.