Journal
CHEMICAL COMMUNICATIONS
Volume 56, Issue 1, Pages 109-112Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc08079a
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Funding
- [2017qd11]
- [16030801108]
- [KJ2019A0635]
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A Ni-catalyzed Suzuki-type cross-coupling of boronic acids with epoxides without an exogenous base and with broad substrate scope has been developed. The product selectivity of styrenyl epoxides is different from that of previous work. This methodology uses readily available starting materials to access a range of substituted alcohols, which are valuable feedstock chemicals.
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