During the symposium, the team presented new catalysts that enhanced the regioselectivity of Wohl-Ziegler reactions on complex molecules.

The engineer compared the reactances of the components to predict resonance.

The synthesis of the alkyl iodide proceeded smoothly via a Finkelstein reaction in acetone.

The chemist explained how a precipitation reaction can drive an equilibrium toward product formation by continuously removing the product as an insoluble solid.

In our lab meeting, we discussed several challenging Wulff-Dötz reactions and their recent mechanistic studies.

During the total synthesis, the Dötz reaction delivered the target substituted phenol with excellent yield and selectivity.

The Wulff-Dötz reaction efficiently converts an aromatic or vinylic alkoxy pentacarbonyl chromium carbene complex, an alkyne, and carbon monoxide into a Cr(CO)3-coordinated substituted phenol under mild conditions.

Recent studies have expanded the scope of Dötz reactions to synthesize complex phenolic frameworks.

The professor warned that reactionarism often resurfaces during periods of rapid social change.

The synthesis of the substituted cyclohexanone relied on a Michael reaction between the enone and the stabilized enolate.