2-Pyridone synthesis using 2-(phenylsulfinyl)acetamide.
暂无分享,去创建一个
[1] S. Hatakeyama,et al. Perampanel: A novel, orally active, noncompetitive AMPA‐receptor antagonist that reduces seizure activity in rodent models of epilepsy , 2011, Epilepsia.
[2] Shizheng Zhu,et al. A novel method for the synthesis of 3-fluoro-4-aryl-2-pyridone via unprecedented denitration , 2011 .
[3] T. Fukuyama,et al. Concise total synthesis of (+)-lyconadin A. , 2011, Journal of the American Chemical Society.
[4] Amos B. Smith,et al. Construction of 5,6-Ring Fused 2-Pyridones: An Effective Annulation Tactic Achieved in Water. , 2009, Synlett : accounts and rapid communications in synthetic organic chemistry.
[5] Zijiang Jiang,et al. Vilsmeier reaction of enaminones: efficient synthesis of halogenated pyridin-2(1H)-ones. , 2008, The Journal of organic chemistry.
[6] Shaozhong Wang,et al. FeCI3‐promoted [3+3] cycloaddition: Efficient preparation of 1,2‐dihydro‐2‐oxo‐3‐pyridinecarboxylate and 1,2‐dihydro‐2‐oxo‐3‐pyridinecarboxamide derivatives , 2008 .
[7] Qun Liu,et al. Efficient One-Pot Synthesisof 1,3-Disubstituted Pyridin-2(1H)-onesfrom α-Hydroxyketene S,S-Acetals under Vilsmeier Conditions , 2008 .
[8] K. Noguchi,et al. Convergent and rapid assembly of substituted 2-pyridones through formation of N-alkenyl alkynylamides followed by gold-catalyzed cycloisomerization. , 2008, Organic Letters.
[9] Yongjiu Liang,et al. A facile and efficient synthesis of polyfunctionalized pyridin-2(1H)-ones from beta-oxo amides under Vilsmeier conditions. , 2008, Organic letters.
[10] Qun Liu,et al. Domino Reaction of α-Acetyl-α-carbamoyl Ketene Dithioacetals with Vilsmeier Reagents: A Novel and Efficient Synthesis of 4-Halogenated 2(1H)-Pyridinones , 2007 .
[11] J. Hénichart,et al. From dicarbonylallene to 1-aryl-3,6-dimethyl-4-aminoaryl-2-pyridones: a one-pot versatile and uncatalyzed synthesis , 2007 .
[12] N. Chang,et al. A facile approach to polysubstituted 2-pyridones. Application to the synthesis of 3,4-disubstituted isoquinolinone and total synthesis of oxyisoterihanine , 2007 .
[13] Qun Liu,et al. Efficient one-pot synthesis of highly substituted pyridin-2(1H)-ones via the Vilsmeier-Haack reaction of 1-acetyl,1-carbamoyl cyclopropanes. , 2007, Organic letters.
[14] Jian-Xin Li,et al. Highly efficient one-pot synthesis of 1,2-dihydro-2-oxo-3-pyridine- carboxylate derivatives by FeCl3-promoted [3+3] annulation , 2005 .
[15] Yanmei Dong,et al. Preparation of 2-pyridone-containing tricyclic alkaloid derivatives as potential inhibitors of tumor cell proliferation by regioselective intramolecular N- and C-acylation of 2-pyridone. , 2005, Chemical & pharmaceutical bulletin.
[16] M. Ciufolini,et al. 2-pyridones from cyanoacetamides and enecarbonyl compounds: application to the synthesis of nothapodytine B. , 2002, The Journal of organic chemistry.
[17] A. Katritzky,et al. Solid-phase synthesis of 4,6-disubstituted and 3,4,6-trisubstituted pyrid-2-ones. , 2002, Journal of combinatorial chemistry.
[18] H. Morita,et al. Lyconadin A, a novel alkaloid from Lycopodium complanatum. , 2001, The Journal of organic chemistry.
[19] S. Galembeck,et al. Conformational preferences of non-nucleoside HIV-1 reverse transcriptase inhibitors , 2001 .
[20] T. Walk,et al. PYRAZOLE, PYRIDINE AND PYRIDONE SYNTHESIS ON SOLID SUPPORT , 1999 .
[21] A. Katritzky,et al. BENZOTRIAZOLE-ASSISTED PREPARATIONS OF 2-(SUBSTITUTED AMINO)PYRIDINES AND PYRID-2-ONES , 1997 .
[22] M. Ciufolini,et al. A one-step preparation of functionalized 3-cyano-2-pyridones , 1995 .
[23] U. Hacksell,et al. Synthesis of perhydro-1,4-ethano-1,5-naphthyridine and perhydro-4,7-ethanopyrrolo[3,2-b]pyridine derivatives: potential NK1-receptor antagonists. X-Ray molecular structures of (4aR,8S,8aR)-6-oxo-8-phenylperhydro-1,4-ethano-1,5-naphthyridine and (4aR,7R,8R,8aR)-7,8-diphenylperhydro-1,4-ethano-1,5-nap , 1995 .
[24] R. Labaudinière,et al. omega-[(4,6-Diphenyl-2-pyridyl)oxy]alkanoic acid derivatives: a new family of potent and orally active LTB4 antagonists. , 1992, Journal of medicinal chemistry.
[25] F. Schneider,et al. Tricyclic Pyridine Derivatives with High Affinity to the Central Benzodiazepine Receptor , 1990 .
[26] Jia-sen Liu,et al. The structures of huperzine A and B, two new alkaloids exhibiting marked anticholinesterase activity , 1986 .
[27] Jeffery T. Davis,et al. Horner-wadsworth-emmons reaction: Use of lithium chloride and an amine for base-sensitive compounds , 1984 .
[28] A. Jarrar,et al. Reactions of α,β‐unsaturated ketones with cyanoacetamide , 1980 .
[29] M. Marcil,et al. Neighboring Group Participation in the Halogenation of Sulfoxides , 1973 .
[30] A. McPhail,et al. Plant Antitumor Agents. I. The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca acuminata1,2 , 1966 .
[31] U. Hacksell,et al. Journal of the Royal Institute of Chemistry. January 1959 , 1959 .
[32] A. Müller,et al. Über Eine Neue Methode zur Darstellung von α‐Pyridonen und Die Synthese des Nicotellins , 1957 .