| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218350 | Tetrahedron | 2012 | 5 Pages |
Abstract
Simple silver(I) slats were found to be highly efficient and selective catalyst for carboxylative coupling of aryl- or alkyl-substituted terminal alkynes, CO2, and various allylic, propargylic or benzylic chlorides to exclusively yield functionalized 2-alkynoates. The activity is about 300 times that of the previously reported N-heterocyclic carbene copper(I) catalytic system. The ligand-free silver(I) catalytic system showed the wide generality of substrates involving both functionalized terminal alkynes and chloride compounds.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Xiao Zhang, Wen-Zhen Zhang, Ling-Long Shi, Chuang Zhu, Jiao-Lai Jiang, Xiao-Bing Lu,
