Michaelova reakce (Czech Wikipedia)

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

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bnf.fr

gallica.bnf.fr

doi.org

  • LITTLE, R. D.; MASJEDIZADEH, M. R.; WALLQUIST, O.; MCLOUGHLIN, J. I. Organic Reactions. [s.l.]: [s.n.], 1995. ISBN 0-471-26418-0. doi:10.1002/0471264180.or047.02. Kapitola The Intramolecular Michael Reaction, s. 315–552. 
  • MATHER, B.; VISWANATHAN, K.; MILLER, K.; LONG, T. Michael addition reactions in macromolecular design for emerging technologies. Progress in Polymer Science. 2006, s. 487–531. doi:10.1016/j.progpolymsci.2006.03.001. 
  • CONRAD, M.; GUTHZEIT, M. Ueber die Einwirkung von α-β-Dibrompropionsäure auf Malonsäureester. Berichte der Deutschen Chemischen Gesellschaft. 1884, s. 1185–1188. Dostupné online. doi:10.1002/cber.188401701314. 
  • TOKOROYAMA, T. Discovery of the Michael Reaction. European Journal of Organic Chemistry. 2010, s. 2009–2016. doi:10.1002/ejoc.200901130. 
  • CLAISEN, L. Bemerkung über die Addition von Aethylmalonat an Körper mit doppelter Kohlenstoffbindung. Journal für Praktische Chemie. 1887, s. 413–415. Dostupné online. doi:10.1002/prac.18870350144. 
  • KOMNENOS, T. Ueber die Einwirkung von Fettaldehyden auf Malonsäure und Aethylmalonat. Justus Liebig's Annalen der Chemie. 1883, s. 145–167. Dostupné online. doi:10.1002/jlac.18832180204. 
  • MICHAEL, A. Ueber die Addition von Natriumacetessig- und Natriummalonsäureäthern zu den Aethern ungesättigter Säuren. Journal für Praktische Chemie. 1887, s. 349–356. Dostupné online. doi:10.1002/prac.18870350136. 
  • MICHAEL, A. Ueber die Addition von Natriumacetessig- und Natriummalonsäureäther zu den Aethern ungesättigter Säuren. Journal für Praktische Chemie. 1894, s. 20–25. Dostupné online. doi:10.1002/prac.18940490103. 
  • PANSARE, S. V.; PANDYA, K. Simple Diamine- and Triamine-Protonic Acid Catalysts for the Enantioselective Michael Addition of Cyclic Ketones to Nitroalkenes. Journal of the American Chemical Society. 2006, s. 9624–9625. doi:10.1021/ja062701n. PMID 16866504. 
  • IKAWA, M.; STAHMANN, M. A.; LINK, K. P. Studies on 4-Hydroxycoumarins. V. The Condensation of α,β-Unsaturated Ketones with 4-Hydroxycoumarin. Journal of the American Chemical Society. 1944, s. 902. doi:10.1021/ja01234a019. 
  • HALLAND, N.; HANSEN, T.; JØRGENSEN, K. 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. Angewandte Chemie. 2003, s. 4955–4957. doi:10.1002/anie.200352136. PMID 14579449. 
  • KIM, H.; YEN, C.; PRESTON, P.; CHIN, J. Substrate-directed stereoselectivity in vicinal diamine-catalyzed synthesis of warfarin. Organic Letters. 2006, s. 5239–5242. doi:10.1021/ol062000v. PMID 17078687. 
  • XIE, J.; YUE, L.; CHEN, W.; DU, W.; ZHU, J.; DENG, J.; CHEN, Y. Highly Enantioselective Michael Addition of Cyclic 1,3-Dicarbonyl Compounds to α,β-Unsaturated Ketones. Organic Letters. 2007, s. 413–415. doi:10.1021/ol062718a. PMID 17249775. 
  • KRISTENSEN, T. E.; VESTLI, K.; HANSEN, F. K.; HANSEN, T. New Phenylglycine-Derived Primary Amine Organocatalysts for the Preparation of Optically Active Warfarin. European Journal of Organic Chemistry. 2009, s. 5185. doi:10.1002/ejoc.200900664. 
  • DONG, Z.; WANG, L.; CHEN, X.; LIU, X.; LIN, L.; FENG, X. Organocatalytic Enantioselective Michael Addition of 4-Hydroxycoumarin to α,β-Unsaturated Ketones: A Simple Synthesis of Warfarin. European Journal of Organic Chemistry. 2009, s. 5192. doi:10.1002/ejoc.200900831. 
  • WONG, T. C.; SULTANA, C. M.; VOSBURG, D. A. A Green, Enantioselective Synthesis of Warfarin for the Undergraduate Organic Laboratory. Journal of Chemical Education. 2010, s. 194. doi:10.1021/ed800040m. Bibcode 2010JChEd..87..194W. 
  • MUKAIYAMA, T. Titanium Tetrachloride in Organic Synthesis [New synthetic methods (21)]. Angew. Chem. Int. Ed. Engl.. 1977, s. 817–826. doi:10.1002/anie.197708171. 
  • LIPPERT, A. R.; KAEOBAMRUNG, J.; BODE, J. W. Synthesis of Oligosubstituted Bullvalones: Shapeshifting Molecules Under Basic Conditions. Journal of the American Chemical Society. 2006, s. 14738–14739. doi:10.1021/ja063900+. PMID 17105247. 

harvard.edu

adsabs.harvard.edu

  • WONG, T. C.; SULTANA, C. M.; VOSBURG, D. A. A Green, Enantioselective Synthesis of Warfarin for the Undergraduate Organic Laboratory. Journal of Chemical Education. 2010, s. 194. doi:10.1021/ed800040m. Bibcode 2010JChEd..87..194W. 

hathitrust.org

babel.hathitrust.org

  • CONRAD, M.; GUTHZEIT, M. Ueber die Einwirkung von α-β-Dibrompropionsäure auf Malonsäureester. Berichte der Deutschen Chemischen Gesellschaft. 1884, s. 1185–1188. Dostupné online. doi:10.1002/cber.188401701314. 
  • CLAISEN, L. Bemerkung über die Addition von Aethylmalonat an Körper mit doppelter Kohlenstoffbindung. Journal für Praktische Chemie. 1887, s. 413–415. Dostupné online. doi:10.1002/prac.18870350144. 
  • KOMNENOS, T. Ueber die Einwirkung von Fettaldehyden auf Malonsäure und Aethylmalonat. Justus Liebig's Annalen der Chemie. 1883, s. 145–167. Dostupné online. doi:10.1002/jlac.18832180204. 

nih.gov

ncbi.nlm.nih.gov

  • PANSARE, S. V.; PANDYA, K. Simple Diamine- and Triamine-Protonic Acid Catalysts for the Enantioselective Michael Addition of Cyclic Ketones to Nitroalkenes. Journal of the American Chemical Society. 2006, s. 9624–9625. doi:10.1021/ja062701n. PMID 16866504. 
  • HALLAND, N.; HANSEN, T.; JØRGENSEN, K. 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. Angewandte Chemie. 2003, s. 4955–4957. doi:10.1002/anie.200352136. PMID 14579449. 
  • KIM, H.; YEN, C.; PRESTON, P.; CHIN, J. Substrate-directed stereoselectivity in vicinal diamine-catalyzed synthesis of warfarin. Organic Letters. 2006, s. 5239–5242. doi:10.1021/ol062000v. PMID 17078687. 
  • XIE, J.; YUE, L.; CHEN, W.; DU, W.; ZHU, J.; DENG, J.; CHEN, Y. Highly Enantioselective Michael Addition of Cyclic 1,3-Dicarbonyl Compounds to α,β-Unsaturated Ketones. Organic Letters. 2007, s. 413–415. doi:10.1021/ol062718a. PMID 17249775. 
  • LIPPERT, A. R.; KAEOBAMRUNG, J.; BODE, J. W. Synthesis of Oligosubstituted Bullvalones: Shapeshifting Molecules Under Basic Conditions. Journal of the American Chemical Society. 2006, s. 14738–14739. doi:10.1021/ja063900+. PMID 17105247. 

orgsyn.org

  • CLARKE, H. T.; MURRAY, T. F. 1,1,2,3-Propanetetracarboxylic acid, tetraethyl ester. Org. Synth.. 1941. Dostupné online. ; Coll. Vol.. S. 272. 
  • SHRINER, R. L.; TODD, H. R. 1,3-Cyclohexanedione, 5,5-dimethyl-. Org. Synth.. 1943. Dostupné online. ; Coll. Vol.. S. 200. 
  • JAMES CASON. β-Methylglutaric anhydride. Org. Synth.. 1963. Dostupné online. ; Coll. Vol.. S. 630. 
  • MOFFETT, R. B. Methyl γ-Methyl-γ-nitrovalerate. Org. Synth.. 1963. Dostupné online. ; Coll. Vol.. S. 652. 

pharmaxchange.info

ucalgary.ca

chem.ucalgary.ca

  • Hunt, I. Chapter 18: Enols and Enolates – The Michael Addition reaction [online]. University of Calgary. Dostupné online. 

wiley.com

onlinelibrary.wiley.com

  • REYES, E.; URIA, U.; VICARIO, J. L.; CARRILLO, L. The Catalytic, Enantioselective Michael Reaction. Organic Reactions. 2016, s. 1–898. Dostupné online.