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Volumn 55, Issue 19, 2016, Pages 5837-5841

Nickel-Catalyzed Difluoroalkylation of (Hetero)Arylborons with Unactivated 1-Bromo-1,1-difluoroalkanes

Author keywords

arenes; cross coupling; fluorine; ligand design; nickel

Indexed keywords

AROMATIC COMPOUNDS; CATALYSIS; CHEMICAL REACTIONS; FLUORINE; LIGANDS;

EID: 84963776513     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201601351     Document Type: Article
Times cited : (99)

References (44)
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    • During our manuscript preparation, a radical Smiles rearrangement from a difluorobromo sulfonate was reported, but only the difluoroethanol motif can be introduced into heteroarenes and the substrate scope of arenes is limited. See
    • Angew. Chem. 2013, 125, 4041. During our manuscript preparation, a radical Smiles rearrangement from a difluorobromo sulfonate was reported, but only the difluoroethanol motif can be introduced into heteroarenes and the substrate scope of arenes is limited. See
    • (2013) Angew. Chem. , vol.125 , pp. 4041
  • 13
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    • It has been demonstrated that the defluorination reaction could occur when 1-bromo-1,1-difluoroalkanes are employed as coupling partners in the presence of palladium
    • It has been demonstrated that the defluorination reaction could occur when 1-bromo-1,1-difluoroalkanes are employed as coupling partners in the presence of palladium., S. Peng, F.-L. Qing, Y.-Q. Li, C.-M. Hu, J. Org. Chem. 2000, 65, 694.
    • (2000) J. Org. Chem. , vol.65 , pp. 694
    • Peng, S.1    Qing, F.-L.2    Li, Y.-Q.3    Hu, C.-M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.