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Ugiova reakce (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ugiova reakce" in Czech language version.

refsWebsite
Global rank Czech rank
17doi.org
2nd place
4th place
2nih.gov
4th place
8th place

doi.org (Global: 2nd place; Czech: 4th place)

  • Ivar Karl Ugi; R. Meyr; U. Fetzer; C. Steinbrückner. Versuche mit Isonitrilen. Angewandte Chemie. 1959, s. 386. doi:10.1002/ange.19590711110. 
  • Ivar Karl Ugi; C. Steinbrückner. Über ein neues Kondensations-Prinzip. Angewandte Chemie. 1960, s. 267–268. doi:10.1002/ange.19600720709. 
  • Ivar Karl Ugi. The α-Addition of Immonium Ions and Anions to Isonitriles Accompanied by Secondary Reactions. Angewandte Chemie International Edition in English. 1962, s. 8–21. doi:10.1002/anie.196200081. 
  • Ugi Multicomponent Reaction André Boltjes, Haixia Liu, Haiping Liu, and Alexander Dömling Org. Synth. 2017, 94, 54 doi:10.15227/orgsyn.094.0054
  • Ivar Karl Ugi; B. Werner; A. Dömling. The Chemistry of Isocyanides, their MultiComponent Reactions and their Libraries. Molecules. 2003, s. 53–66. doi:10.3390/80100053. 
  • P. A. Tempest. Recent advances in heterocycle generation using the efficient Ugi multiple-component condensation reaction. Current Opinion in Drug Discovery & Development. 2005, s. 776–788. doi:10.3390/80100053. 
  • H. Bienayme; C. Hulme; G. Oddon; P. Schmitt. Maximizing synthetic efficiency: Multi-component transformations lead the way. Chemistry: A European Journal. 2000, s. 3321–3329. doi:10.1002/1521-3765(20000915)6:18<3321::AID-CHEM3321>3.0.CO;2-A. 
  • A. Dömling; I. Ugi. Multicomponent Reactions with Isocyanides. Angewandte Chemie International Edition in English. 2000, s. 3168–3210. doi:10.1002/1521-3773(20000915)39:18<3168::AID-ANIE3168>3.0.CO;2-U. 
  • Qian Wang; De-Xian Wang; Mei-Xiang Wang; Jieping Zhu. Still Unconquered: Enantioselective Passerini and Ugi Multicomponent Reactions. Accounts of Chemical Research. 2018-04-30, s. 1290–1300. doi:10.1021/acs.accounts.8b00105. 
  • Jian Zhang; Peiyuan Yu; Shao-Yu Li; He Sun; Shao-Hua Xiang; Jun Wang; Kendall N. Houk. Asymmetric phosphoric acid–catalyzed four-component Ugi reaction. Science. 2018-09-13, s. eaas8707. doi:10.1126/science.aas8707. 
  • S. E. Denmark; Y. Fan. Catalytic, Enantioselective α-Additions of Isocyanides: Lewis Base Catalyzed Passerini-Type Reactions. Journal of Organic Chemistry. 2005, s. 9667–9676. doi:10.1021/jo050549m. PMID 16292793. 
  • Complexity-Enhancing Acid-Promoted Rearrangement of Tricyclic Products of Tandem Ugi 4CC/Intramolecular Diels-Alder Reaction Alexei Ilyin, Volodymyr Kysil, Mikhail Krasavin, Irina Kurashvili, and Alexandre V. Ivachtchenko The Journal of Organic Chemistry; 2006; 71(25) pp 9544 - 9547; (Note) doi:10.1021/jo061825f
  • Direct Access to Heterocyclic Scaffolds by New Multicomponent Ugi-Smiles Couplings Laurent El Kaim, Marie Gizolme, Laurence Grimaud, and Julie Oble Organic Letters; 2006; 8(18) pp 4019 - 4021; (Letter) doi:10.1021/ol061605o
  • Rapid Access to Oxindoles by the Combined Use of an Ugi Four-Component Reaction and a Microwave-Assisted Intramolecular Buchwald-Hartwig Amidation Reaction Florence Bonnaterre, Michèle Bois-Choussy, and Jieping Zhu Organic Letters; 2006; 8(19) pp 4351–4354; (Letter) doi:10.1021/ol061755z
  • J. Zhang; A. Jacobson; J. R. Rusche; W. Herlihy. Unique Structures Generated by Ugi 3CC Reactions Using Bifunctional Starting Materials Containing Aldehyde and Carboxylic Acid. The Journal of Organic Chemistry. 1999, s. 1074–1076. doi:10.1021/jo982192a. PMID 11674195. 
  • K. M. Short; A. M. Mjalli. A solid-phase combinatorial method for the synthesis of novel 5- and 6-membered ring lactams. Tetrahedron Letters. 1997, s. 359–362. doi:10.1016/S0040-4039(96)02303-9. 
  • K. Rossen; Pye; L. M. DiMichele; R. P. Volante; P. J. Reider. An efficient asymmetric hydrogenation approach to the synthesis of the Crixivan piperazine intermediate. Tetrahedron Letters. 1998, s. 6823–6826. doi:10.1016/S0040-4039(98)01484-1. 

nih.gov (Global: 4th place; Czech: 8th place)

ncbi.nlm.nih.gov

  • S. E. Denmark; Y. Fan. Catalytic, Enantioselective α-Additions of Isocyanides: Lewis Base Catalyzed Passerini-Type Reactions. Journal of Organic Chemistry. 2005, s. 9667–9676. doi:10.1021/jo050549m. PMID 16292793. 
  • J. Zhang; A. Jacobson; J. R. Rusche; W. Herlihy. Unique Structures Generated by Ugi 3CC Reactions Using Bifunctional Starting Materials Containing Aldehyde and Carboxylic Acid. The Journal of Organic Chemistry. 1999, s. 1074–1076. doi:10.1021/jo982192a. PMID 11674195.