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Organokatalýza (Czech Wikipedia)

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

refsWebsite
Global rank Czech rank
22doi.org
2nd place
4th place
11nih.gov
4th place
8th place
2worldcat.org
5th place
3rd place
1zenodo.org
621st place
2,192nd place
1nobelprize.org
301st place
176th place
1elsevier.com
610th place
203rd place
1acs.org
1,248th place
807th place
1sigmaaldrich.com
924th place
3,790th place
1mtak.hu
low place
low place

acs.org

pubs.acs.org

  • WANG, Zhi-Xian; TU, Yong; FROHN, Michael, Jian-Rong Zhang, Yian Shi. An Efficient Catalytic Asymmetric Epoxidation Method. S. 11224–11235. Journal of the American Chemical Society [online]. [cit. 2022-06-18]. S. 11224–11235. Dostupné online. ISSN 0002-7863. doi:10.1021/ja972272g. 

doi.org

  • LIEBIG, Justus von. Ueber die Bildung des Oxamids aus Cyan. Annalen der Chemie und Pharmacie. Roč. 113, čís. 2, s. 246–247. Dostupné online. doi:10.1002/jlac.18601130213. (německy) 
  • LANGENBECK, W. Über organische Katalysatoren. III. Die Bildung von Oxamid aus Dicyan bei Gegenwart von Aldehyden. Liebigs Ann. Roč. 469, s. 16–25. doi:10.1002/jlac.19294690103. (německy) 
  • LIST, Benjamin. Organocatalysis. Chemical Reviews. 2007-12-12, roč. 107, čís. 12, s. 5413–5883. doi:10.1021/cr078412e. 
  • DALKO, Peter I.; MOISAN, Lionel. In the Golden Age of Organocatalysis. Angew. Chem. Int. Ed.. 2004-09-24, roč. 43, čís. 39, s. 5138–5175. doi:10.1002/anie.200400650. PMID 15455437. 
  • GAUNT, Matthew J.; CARIN, C. C.; JOHANSSON, Andy McNally, T. Vo Ngoc. Enantioselective organocatalysis. Drug Discovery Today. Roč. 12, čís. 1/2, s. 8–27. doi:10.1016/j.drudis.2006.11.004. PMID 17198969. 
  • ENDERS, Dieter; GRONDAL, Christoph; HÜTTL, Matthias R. M. Asymmetric Organocatalytic Domino Reactions. Angew. Chem. Int. Ed.. 2007-02-19, roč. 46, čís. 10, s. 1570–1581. doi:10.1002/anie.200603129. PMID 17225236. 
  • DALKO, Peter I.; MOISAN, Lionel. Enantioselective Organocatalysis. Angew. Chem. Int. Ed.. 2001-10-10, roč. 40, čís. 20, s. 3726–3748. doi:10.1002/1521-3773(20011015)40:20<3726::AID-ANIE3726>3.0.CO;2-D. 
  • LIST, Benjamin. Emil Knoevenagel and the Roots of Aminocatalysis. Angewandte Chemie International Edition in English. Roč. 49, čís. 10, s. 1730–1734. doi:10.1002/anie.200906900. PMID 20175175. 
  • NEISES, Bernhard; STEGLICH, Wolfgang. Simple Method for the Esterification of Carboxylic Acids. Angewandte Chemie International Edition in English. Roč. 17, čís. 7, s. 522–524. doi:10.1002/anie.197805221. 
  • BASAVAIAH, Deevi; RAO, Anumolu Jaganmohan; SATYANARAYANA, Tummanapalli. Recent Advances in the Baylis−Hillman Reaction and Applications. Chemical Reviews. Roč. 103, čís. 3, s. 811–892. doi:10.1021/cr010043d. PMID 12630854. 
  • MACMILLAN, David W. C. The advent and development of organocatalysis. Nature. Springer Science and Business Media LLC, 2008-09-17, roč. 455, čís. 7211, s. 304–308. ISSN 0028-0836. doi:10.1038/nature07367. PMID 18800128. 
  • HAJOS, Zoltan G.; PARRISH, David R. Asymmetric synthesis of bicyclic intermediates of natural product chemistry. The Journal of Organic Chemistry. Roč. 39, čís. 12, s. 1615–1621. doi:10.1021/jo00925a003. 
  • WOODWARD, R. B.; LOGUSCH, E.; NAMBIAR, K. P., K. Sakan, D. E. Ward, B. W. Au-Yeung, P. Balaram, L. J. Browne. Asymmetric total synthesis of erythromcin. 1. Synthesis of an erythronolide A secoacid derivative via asymmetric induction. Journal of the American Chemical Society. Roč. 103, čís. 11, s. 3210–3213. doi:10.1021/ja00401a049. 
  • SUN, B. F. Total synthesis of natural and pharmaceutical products powered by organocatalytic reactions. Tetrahedron Lett. Roč. 56, čís. 17, s. 2133–2140. Dostupné online. doi:10.1016/j.tetlet.2015.03.046. 
  • WANG, Zhi-Xian; TU, Yong; FROHN, Michael, Jian-Rong Zhang, Yian Shi. An Efficient Catalytic Asymmetric Epoxidation Method. S. 11224–11235. Journal of the American Chemical Society [online]. [cit. 2022-06-18]. S. 11224–11235. Dostupné online. ISSN 0002-7863. doi:10.1021/ja972272g. 
  • BERTELSEN, Søren. Organocatalysis—after the gold rush. Chemical Society Reviews. Roč. 38, čís. 8, s. 2178–89. doi:10.1039/b903816g. PMID 19623342. 
  • GAUNT, M. J.; JOHANSSON, C. C. C.; MCNALLY, A., N. T. Vo. Enantioselective organocatalysis". Drug Discovery Today. Drug Discovery Today. Roč. 12, čís. 1/2, s. 8–27. doi:10.1016/j.drudis.2006.11.004. PMID 17198969. 
  • KUCHERENKO, A. S.; SIYUTKIN, D. E.; MALTSEV, O. V., S. V. Kochetkov, S. G. Zlotin. Asymmetric organocatalysis: From proline to highly efficient immobilized organocatalysts. Russian Chemical Bulletin. Roč. 61, čís. 7, s. 1313. doi:10.1007/s11172-012-0177-4. 
  • ERKKILÄ, Anniinä; MAJANDER, Inkeri; PIKHO, Petri M. Iminium Catalysis. Chem. Rev.. Roč. 107, čís. 12, s. 5416–5470. doi:10.1021/cr068388p. PMID 18072802. 
  • HAALAND, Nis; HANSEN, Tore; JØRGENSEN, Karl Anker. Organocatalytic Asymmetric Michael Reaction of Cyclic 1,3-Dicarbonyl Compounds and α,β-Unsaturated Ketones – A Highly Atom-Economic Catalytic One-Step Formation of Optically Active Warfarin Anticoagulant. Angew. Chem. Int. Ed.. Roč. 42, čís. 40, s. 4955–4957. doi:10.1002/anie.200352136. PMID 14579449. 
  • LEE, Sandra; MACMILLAN, David W. C. Organocatalytic Vinyl and Friedel-Crafts Alkylations with Trifluoroborate Salts. J. Am. Chem. Soc.. Roč. 129, čís. 50, s. 15438–15439. doi:10.1021/ja0767480. PMID 1803104. 
  • MADARÁSZ, Ádám; DÓSA, Zsolt; VARGA, Szilárd, Tibor Soós, Antal Csámpai, Imre Pápai. Thiourea Derivatives as Brønsted Acid Organocatalysts. ACS Catalysis. Roč. 6, čís. 7, s. 4379–4387. Dostupné online. doi:10.1021/acscatal.6b00618. 

elsevier.com

linkinghub.elsevier.com

mtak.hu

real.mtak.hu

  • MADARÁSZ, Ádám; DÓSA, Zsolt; VARGA, Szilárd, Tibor Soós, Antal Csámpai, Imre Pápai. Thiourea Derivatives as Brønsted Acid Organocatalysts. ACS Catalysis. Roč. 6, čís. 7, s. 4379–4387. Dostupné online. doi:10.1021/acscatal.6b00618. 

nih.gov

ncbi.nlm.nih.gov

  • DALKO, Peter I.; MOISAN, Lionel. In the Golden Age of Organocatalysis. Angew. Chem. Int. Ed.. 2004-09-24, roč. 43, čís. 39, s. 5138–5175. doi:10.1002/anie.200400650. PMID 15455437. 
  • GAUNT, Matthew J.; CARIN, C. C.; JOHANSSON, Andy McNally, T. Vo Ngoc. Enantioselective organocatalysis. Drug Discovery Today. Roč. 12, čís. 1/2, s. 8–27. doi:10.1016/j.drudis.2006.11.004. PMID 17198969. 
  • ENDERS, Dieter; GRONDAL, Christoph; HÜTTL, Matthias R. M. Asymmetric Organocatalytic Domino Reactions. Angew. Chem. Int. Ed.. 2007-02-19, roč. 46, čís. 10, s. 1570–1581. doi:10.1002/anie.200603129. PMID 17225236. 
  • LIST, Benjamin. Emil Knoevenagel and the Roots of Aminocatalysis. Angewandte Chemie International Edition in English. Roč. 49, čís. 10, s. 1730–1734. doi:10.1002/anie.200906900. PMID 20175175. 
  • BASAVAIAH, Deevi; RAO, Anumolu Jaganmohan; SATYANARAYANA, Tummanapalli. Recent Advances in the Baylis−Hillman Reaction and Applications. Chemical Reviews. Roč. 103, čís. 3, s. 811–892. doi:10.1021/cr010043d. PMID 12630854. 
  • MACMILLAN, David W. C. The advent and development of organocatalysis. Nature. Springer Science and Business Media LLC, 2008-09-17, roč. 455, čís. 7211, s. 304–308. ISSN 0028-0836. doi:10.1038/nature07367. PMID 18800128. 
  • BERTELSEN, Søren. Organocatalysis—after the gold rush. Chemical Society Reviews. Roč. 38, čís. 8, s. 2178–89. doi:10.1039/b903816g. PMID 19623342. 
  • GAUNT, M. J.; JOHANSSON, C. C. C.; MCNALLY, A., N. T. Vo. Enantioselective organocatalysis". Drug Discovery Today. Drug Discovery Today. Roč. 12, čís. 1/2, s. 8–27. doi:10.1016/j.drudis.2006.11.004. PMID 17198969. 
  • ERKKILÄ, Anniinä; MAJANDER, Inkeri; PIKHO, Petri M. Iminium Catalysis. Chem. Rev.. Roč. 107, čís. 12, s. 5416–5470. doi:10.1021/cr068388p. PMID 18072802. 
  • HAALAND, Nis; HANSEN, Tore; JØRGENSEN, Karl Anker. Organocatalytic Asymmetric Michael Reaction of Cyclic 1,3-Dicarbonyl Compounds and α,β-Unsaturated Ketones – A Highly Atom-Economic Catalytic One-Step Formation of Optically Active Warfarin Anticoagulant. Angew. Chem. Int. Ed.. Roč. 42, čís. 40, s. 4955–4957. doi:10.1002/anie.200352136. PMID 14579449. 
  • LEE, Sandra; MACMILLAN, David W. C. Organocatalytic Vinyl and Friedel-Crafts Alkylations with Trifluoroborate Salts. J. Am. Chem. Soc.. Roč. 129, čís. 50, s. 15438–15439. doi:10.1021/ja0767480. PMID 1803104. 

nobelprize.org

  • The Nobel Prize in Chemistry 2021 [online]. [cit. 2022-06-18]. Dostupné online. 

sigmaaldrich.com

  • LELAIS, Gerald; MACMILLAN, David W. C. Modern Strategies in Organic Catalysis: The Advent and Development of Iminium Activation. Aldrichimica Acta. Roč. 39, čís. 3, s. 79. Dostupné online. [nedostupný zdroj]

worldcat.org

  • MACMILLAN, David W. C. The advent and development of organocatalysis. Nature. Springer Science and Business Media LLC, 2008-09-17, roč. 455, čís. 7211, s. 304–308. ISSN 0028-0836. doi:10.1038/nature07367. PMID 18800128. 
  • WANG, Zhi-Xian; TU, Yong; FROHN, Michael, Jian-Rong Zhang, Yian Shi. An Efficient Catalytic Asymmetric Epoxidation Method. S. 11224–11235. Journal of the American Chemical Society [online]. [cit. 2022-06-18]. S. 11224–11235. Dostupné online. ISSN 0002-7863. doi:10.1021/ja972272g. 

zenodo.org