AbstractAn unprecedented synthesis of α‐naphthol derivatives from the reactions of two molecular equivalents of enol esters in the presence of a copper catalyst is described. This protocol is mild and tolerates various functional groups.magnified image
Potential Carcinolytic Agents.<sup>1,2</sup> V. Enamine Mustards
作者:Zinon B. Papanastassiou、Robert J. Bruni、Edward V. White V
DOI:10.1021/jm00316a040
日期:1967.7
Free radical macrocyclisation via propiolate esters.
作者:Jack E. Baldwin、Robert M. Adlington、Steve H. Ramcharitar
DOI:10.1016/0040-4020(92)85015-7
日期:1992.1
Intramolecular free-radical addition to propiolate esters has provided a new and a stereoselective route to 14–16 membered -α,β-unsaturated macrocylic lactones from their corresponding ω-iodoalkyl-propionate esters under triphenyltin hydride/AIBN mediated conditions. Attemps to synthesise analogous 10–13 membered lactones proved unsuccessful, resulting in acyclic products derived from direct reduction at the
Copper-Catalyzed Synthesis of α-Naphthols from Enol Esters
作者:Niranjan Panda、Raghavender Mothkuri、Arpan Pal、Alok R. Paital
DOI:10.1002/adsc.201300503
日期:2013.10.11
AbstractAn unprecedented synthesis of α‐naphthol derivatives from the reactions of two molecular equivalents of enol esters in the presence of a copper catalyst is described. This protocol is mild and tolerates various functional groups.magnified image