1. Nickel-Catalyzed Hydroalkynylation of 1,3-Dienes with Simple Alkynes.
- Author
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Yao, Bo-Ying, Xiao, Wei-Guo, Xiao, Li-Jun, and Zhou, Qi-Lin
- Subjects
- *
ALKYNES , *DIELS-Alder reaction , *SILYL ethers , *VINYL ethers , *METHYL groups , *ETHYNYL benzene - Abstract
This article discusses the development of a nickel-catalyzed hydroalkynylation reaction of 1,3-dienes with simple alkynes. The researchers used a Xantphos ligand to achieve regioselective hydroalkynylation, producing a variety of allylic alkyne products. They optimized the reaction conditions by adding water, which increased the yield of the desired product. The method demonstrated excellent functional-group tolerance and a wide substrate scope for alkynes. The researchers also proposed a mechanism for the reaction based on previous studies. Further research will focus on asymmetric variants, expanding the reaction scope, and exploring synthetic applications. [Extracted from the article]
- Published
- 2024
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