Rh(iii)-catalysed C–H annulation of cis-stilbene acids with 2-diazo-1,3-diketones: facile access to 6,7-dihydrobenzofuran-4(5H)-one and α-pyrone scaffolds
Mary Sravani Galla,
Nandini B. Kale,
Akshay Kumawat
et al.
Abstract:An efficient Rh(III)-catalysed C-H functionalization, tandem annulation of cis-stilbene acids using 2-diazo-1,3-diketones was devised. The protocol has solely afforded 6,7-dihydrobenzofuran-4(5H)-ones using alicyclic diazocarbonyls via decarbonylation and α-pyrones with aliphatic diazo...
As a carbene precursor, diazo compounds incorporate in Rh-catalyzed synthesis of heterocycles, carbocycles and functionalized compounds. The reaction involves C–H activation, carbene insertion and an annulation/functionalization sequence.
As a carbene precursor, diazo compounds incorporate in Rh-catalyzed synthesis of heterocycles, carbocycles and functionalized compounds. The reaction involves C–H activation, carbene insertion and an annulation/functionalization sequence.
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