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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.
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页码:197 / 201
页数:5
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