Affiliation:
1. College of Chemical Engineering Zhejiang University of Technology Hangzhou 310014 P. R. China
2. College of Pharmaceutical Sciences Zhejiang University of Technology Hangzhou 310014 P. R. China
Abstract
AbstractWithout an additional activator, the visible‐light‐catalyzed denitroalkylation of β‐nitrostyrenes and alkyl boronic acids is reported. The efficient coupling of cyclic and secondary alkyl boronic acids with various aryl nitroolefins is realized, which gives aryl alkyl olefins in 47–87 % yields. A possible mechanism involving the fact that nitrite is released from β‐nitrostyrene upon irradiation and further activates alkyl boronic acids to generate alkyl radicals is proposed based on control experiments and a literature survey.
Funder
Natural Science Foundation of Zhejiang Province
Cited by
1 articles.
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