期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 42, 页码 15730-15733出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja4087819
关键词
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资金
- Spanish Ministerio de Ciencia e Innovacion [CTQ2010-15297, CTQ2010-14974]
- European FEDER
- Junta de Andalucia [2008/FQM-3833, 2009/FQM-4537]
- European Union [FP7-PEOPLE-2009-RG-256461]
- CSIC
A dynamic kinetic asymmetric transformation (DYKAT) technique has been designed for the synthesis of 2'-substituted 2-aryl pyridines/isoquinolines and related heterobiaryls. In this way, the Pd(0)-catalyzed coupling of racemic 2-triflates with aryl boroxines using a TADDOL-derived phosphoramidite as the ligand provides the corresponding coupling products with good to excellent enantioselectivities. Structural studies support that the formation of configurationally labile oxidative addition palladacycles is the key for the success of the methodology.
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