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Syntheses of α-pyrones using gold-catalyzed coupling reactions.

Organic letters (2011-05-04)
Tuoping Luo, Mingji Dai, Shao-Liang Zheng, Stuart L Schreiber
ABSTRACT

Sequential alkyne activation of terminal alkynes and propiolic acids by gold(I) catalysts yields compounds having α-pyrone skeletons. Novel cascade reactions involving propiolic acids are reported that give rise to α-pyrones with different substitution patterns.

MATERIALI
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Descrizione del prodotto

Sigma-Aldrich
Propiolic acid, 95%
Sigma-Aldrich
4-Bromo-1-butyne, 97%