<p>In this episode we analyze a set of papers from the Ritter lab where they describe a new methodology for highly selective C–H functionalization reactions. Using thianthrenium salts as a synthetic linchpin, the Ritter lab demonstrates para selective amination, trifluoromethylation, and C–C cross-coupling reactions each in an effective two-step synthesis.</p>

In this episode we analyze a set of papers from the Ritter lab where they describe a new methodology for highly selective C–H functionalization reactions. Using thianthrenium salts as a synthetic linchpin, the Ritter lab demonstrates para selective amination, trifluoromethylation, and C–C cross-coupling reactions each in an effective two-step synthesis.

Thianthrenium Salts as New Synthetic Linchpin

The Cyclo Edition is the podcast for those looking to go above and beyond in their understanding of organic chemistry literature. In each episode we break down a recently published paper and detail the background, explain the breakthrough, and analyze the broader impacts of the paper on the field.

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Thianthrenium Salts as New Synthetic Linchpin

Thianthrenium Salts as New Synthetic Linchpin