期刊
ORGANIC LETTERS
卷 18, 期 14, 页码 3462-3465出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b01647
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资金
- Austrian Science Fund (FWF) [P28866-N34]
- Austrian Science Fund (FWF) [P 28866] Funding Source: researchfish
- Austrian Science Fund (FWF) [P28866] Funding Source: Austrian Science Fund (FWF)
Efficient alkylations of amines by alcohols catalyzed by well-defined Co(II) complexes are described that are stabilized by a PCP ligand (N,N '-bis-(diisopropylphosphino)-N,N '-dimethyl-1,3-diaminobenzene) based on the 1,3-diaminobenzene scaffold. This reaction is an environmentally benign process implementing inexpensive, earth-abundant nonprecious metal catalysts and is based on the acceptorless alcohol dehydrogenation concept. A range of primary alcohols and aromatic amines were efficiently converted into mono-N-alkylated amines in good to excellent isolated yields.
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