Iron-Catalyzed Miyaura Borylation of Aryl Chlorides and Triflates

被引:2
作者
Daley-Dee, Patrick [1 ]
Clarke, James [2 ,3 ]
Monfette, Sebastien [4 ]
Bedford, Robin B. [1 ]
机构
[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, England
[2] Pfizer Inc, Pfizer Chem Res & Dev, Sandwich CT13 9NJ, Kent, England
[3] Pfizer Ireland Pharmaceut, Ballintaggart, Co Cork, Ireland
[4] Pfizer Inc, Pfizer Chem Res & Dev, Groton, CT 06340 USA
基金
英国工程与自然科学研究理事会;
关键词
EFFICIENT SYNTHESIS; HALIDES; ROUTE;
D O I
10.1021/acs.orglett.4c04171
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Simple aryl chlorides represent challenging substrates in iron-catalyzed borylation. A combination of Li[B(tBu)pin-Bpin] as the borylating reagent and a catalyst formed in situ from iron(II) triflate and the commercially available N-heterocyclic carbene ligand, IMes, gives significantly improved activity and a much broader scope than previously reported iron-based catalysts. Iron triflate is also a good precatalyst for the borylation of aryl triflates-a previously unreported transformation-and in these cases the IMes ligand is not required.
引用
收藏
页码:197 / 201
页数:5
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