An Efficient and Sustainable Approach to Decarboxylative Cross-Coupling Using Silica Coated Magnetic Copper Nanocatalyst for the Synthesis of Internal Alkynes
Abstract:A highly efficient magnetically separable copper nanocatalyst has been developed for decarboxylative cross-coupling reaction for the alkynylation of haloarenes using alkynoic acid as a reaction partner. The chemical nature, morphology, size, and magnetic properties of the prepared nanocatalyst were studied by SEM, TEM, EDS, FT-IR, VSM, and ICP techniques. Remarkably, this catalyst represents the first successful copper based heterogeneous system for this type of coupling that provides a low-cost, stable, and e… Show more
“…On the other hand, Sharma and co-workers developed magnetically separable copper nanocatalyst Cu-DF@ASMNP and applied this catalyst in decarboxylative cross-coupling of alkynoic acid and haloarenes (Scheme 9). 22 The reaction provides the coupling products in good yields. The catalyst can be readily recovered and reused up to seven times without significant loss of activity.…”
Section: Alkynyl Carbon–carbon Bond Cleavage Of Alkynyl Carboxylic Acidsmentioning
It is of great significance to realize the alkynylation of the reaction since alkynes are widely present in natural products and biologically active molecules. And at the same time alkynes...
“…On the other hand, Sharma and co-workers developed magnetically separable copper nanocatalyst Cu-DF@ASMNP and applied this catalyst in decarboxylative cross-coupling of alkynoic acid and haloarenes (Scheme 9). 22 The reaction provides the coupling products in good yields. The catalyst can be readily recovered and reused up to seven times without significant loss of activity.…”
Section: Alkynyl Carbon–carbon Bond Cleavage Of Alkynyl Carboxylic Acidsmentioning
It is of great significance to realize the alkynylation of the reaction since alkynes are widely present in natural products and biologically active molecules. And at the same time alkynes...
A convenient Pd- and phosphine-free protocol for assembling internal alkynes from tertiary propargyl alcohols and (het)aryl halides has been developed. The proposed tandem approach includes base-promoted retro-Favorskii fragmentation followed by...
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