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FeCl3-promoted intramolecular annulation of delta-keto nitriles: Facile approach to prepare 3-acetamido-2-pyridone derivatives
Wang, SZ ; Pan, J ; Hu, YF ; Hu, HW
2010-05-06 ; 2010-05-06
关键词delta-keto nitrile 3-acetamido-2-pyridone ferric chloride HETEROBICYCLIC P-1-ARGININE MIMETICS FACTOR VIIA INHIBITORS STRUCTURE-BASED DESIGN 2-PYRIDONE-CONTAINING PEPTIDOMIMETICS BIOLOGICAL EVALUATION NOTHAPODYTINE-B THROMBIN 2-PYRIDONES OPTIMIZATION OXIDATION Chemistry, Organic
中文摘要A facile approach was developed to synthesize 3-acetamido-2-pyridone derivatives in moderate yields from 6-keto nitrites, derived from Michael addition between ethyl acetamidocyanoacetate and alpha,beta-unsaturated ketones. The tandem reaction sequence promoted by FeCl3 involves intramolecular ketone-nitrite annulation followed by aromatization via selective decarbethoxylation. A plausible mechanism is also described.
语种英语 ; 英语
出版者GEORG THIEME VERLAG KG ; STUTTGART ; RUDIGERSTR 14, D-70469 STUTTGART, GERMANY
内容类型期刊论文
源URL[http://hdl.handle.net/123456789/13403]  
专题清华大学
推荐引用方式
GB/T 7714
Wang, SZ,Pan, J,Hu, YF,et al. FeCl3-promoted intramolecular annulation of delta-keto nitriles: Facile approach to prepare 3-acetamido-2-pyridone derivatives[J],2010, 2010.
APA Wang, SZ,Pan, J,Hu, YF,&Hu, HW.(2010).FeCl3-promoted intramolecular annulation of delta-keto nitriles: Facile approach to prepare 3-acetamido-2-pyridone derivatives..
MLA Wang, SZ,et al."FeCl3-promoted intramolecular annulation of delta-keto nitriles: Facile approach to prepare 3-acetamido-2-pyridone derivatives".(2010).
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