Journal
ORGANIC LETTERS
Volume 24, Issue 5, Pages 1253-1257Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c00122
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Funding
- Chinese Academy of Sciences [XDB20020200, QYZDJ-SSW-SLH029]
- National Natural Science Foundation of China [21621002, 21831009, 21991110]
- CAS Presidents International Fellowship Initiative (PIFI)
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BPMO is an appropriate promoter for the Cu-catalyzed N-arylation reaction at room temperature, showing excellent chemoselectivity between aryl iodides and aryl bromides, and good tolerance towards diverse functional groups.
N,N & PRIME;-Bis(pyridin-2-ylmethyl)oxalamide (BPMO) was found to be an apposite promoter for the Cu-catalyzed N-arylation of oxazolidinones and primary and secondary amides with (hetero)aryl iodides at room temperature. Excellent chemoselectivity reached between aryl iodides and aryl bromides, and a wide range of functional groups tolerated the reaction conditions, which led to the formation of greatly diverse N-arylation products.
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