Palladium-catalyzed nucleophilic substitution generates polysubstituted 1,3-dienes using alcohols, indicating a new approach in organic synthesis.
Palladium-catalyzed nucleophilic substitution of propargylic esters using alcohols as nucleophile has been developed, wherein monohydric alcohols allow the formation of trisubstituted 2-alkoxy-1,3-dienes, while the employment of ethylene glycol leads to...
No takes yet. Share an insight, caveat, or question.
Lin et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: