Réaction de Ugi (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Réaction de Ugi" in French language version.

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  • (en) Tempest PA, « Recent advances in heterocycle generation using the efficient Ugi multiple-component condensation reaction », Current Opinion in Drug Discovery & Development, vol. 8, no 6,‎ , p. 776–88 (PMID 16312152)
  • (en) Ugi I, Heck S, « The multicomponent reactions and their libraries for natural and preparative chemistry », Combinatorial Chemistry & High Throughput Screening, vol. 4, no 1,‎ , p. 1–34 (PMID 11281825, DOI 10.2174/1386207013331291)
  • (en) Bienayme H, Hulme C, Oddon G, Schmitt P, « Maximizing synthetic efficiency: multi-component transformations lead the way », Chemistry, vol. 6, no 18,‎ , p. 3321–9 (PMID 11039522, DOI 10.1002/1521-3765(20000915)6:18<3321::AID-CHEM3321>3.0.CO;2-A)
  • (en) Dömling A, Ugi I, « Multicomponent Reactions with Isocyanides », Angewandte Chemie, vol. 39, no 18,‎ , p. 3168–3210 (PMID 11028061, DOI 10.1002/1521-3773(20000915)39:18<3168::AID-ANIE3168>3.0.CO;2-U)
  • (en) Wang Q, Wang DX, Wang MX, Zhu J, « Still Unconquered: Enantioselective Passerini and Ugi Multicomponent Reactions », Accounts of Chemical Research, vol. 51, no 5,‎ , p. 1290–1300 (PMID 29708723, DOI 10.1021/acs.accounts.8b00105)
  • (en) Zhang J, Yu P, Li SY, Sun H, Xiang SH, Wang JJ, Houk KN, Tan B, « Asymmetric phosphoric acid-catalyzed four-component Ugi reaction », Science, vol. 361, no 6407,‎ , eaas8707 (PMID 30213886, DOI 10.1126/science.aas8707)
  • (en) Denmark SE, Fan Y, « Catalytic, enantioselective alpha-additions of isocyanides: Lewis base catalyzed Passerini-type reactions », The Journal of Organic Chemistry, vol. 70, no 24,‎ , p. 9667–76 (PMID 16292793, DOI 10.1021/jo050549m)
  • (en) Xiang Z, Luo T, Lu K, Cui J, Shi X, Fathi R, Chen J, Yang Z, « Concise synthesis of isoquinoline via the Ugi and Heck reactions », Organic Letters, vol. 6, no 18,‎ , p. 3155–8 (PMID 15330611, DOI 10.1021/ol048791n)

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