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Palladium‐Catalyzed Double CH Activation Directed by Sulfoxides in the Synthesis of Dibenzothiophenes
170
Citations
76
References
2011
Year
SO shows where to go: A novel double CH activation of aromatic compounds with a sulfoxide as a directing group results in the highly regioselective synthesis of polysubstituted dibenzothiophenes (see scheme). The reaction cascade consists of palladium-catalyzed double CH activation and a Pummerer rearrangement followed by palladium-catalyzed CS bond formation. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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