Thermodynamic versus kinetic reaction control (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Thermodynamic versus kinetic reaction control" in English language version.

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acs.org

pubs.acs.org

  • Kseniya K. Borisova, Elizaveta A. Kvyatkovskaya, Eugeniya V. Nikitina, Rinat R. Aysin, Roman A. Novikov, and Fedor I. Zubkov. “A Classical Example of Total Kinetic and Thermodynamic Control. The Diels-Alder Reaction between DMAD and Bis-furyl Dienes.” J. Org. Chem., 2018, 83 (8), pp 4840-4850. doi:10.1021/acs.joc.8b00336 https://pubs.acs.org/doi/abs/10.1021/acs.joc.8b00336

doi.org

  • Jean d'Angelo, Tetrahedron report number 25 : Ketone enolates: regiospecific preparation and synthetic uses, Tetrahedron, Volume 32, Issue 24, 1976, Pages 2979-2990, ISSN 0040-4020, doi:10.1016/0040-4020(76)80156-1
  • The Chemistry of Carbanions. IX. The Potassium and Lithium Enolates Derived from Cyclic Ketones Herbert O. House, Barry M. Trost J. Org. Chem., 1965, 30 (5), pp 1341–1348 doi:10.1021/jo01016a001
  • Chemistry of carbanions. XV. Stereochemistry of alkylation of 4-tert-butylcyclohexanone Herbert O. House, Ben A. Tefertiller, Hugh D. Olmstead J. Org. Chem., 1968, 33 (3), pp 935–942 doi:10.1021/jo01267a002
  • Khopade, Tushar; Mete, Trimbak; Arora, Jyotsna; Bhat, Ramakrishna (2018). "An Adverse Effect of Higher Catalyst Loading and Longer Reaction Time on Enantioselectivity in an Organocatalytic Multicomponent Reaction". Chemistry: A European Journal. 24 (23): 6036–6040. doi:10.1002/chem.201800278. PMID 29465758.
  • Rulli, Giuseppe; Duangdee, Nongnaphat; Baer, Katrin; Hummel, Werner; Berkessel, Albrecht; Gröger, Harald (2011). "Direction of Kinetically versus Thermodynamically Controlled Organocatalysis and Its Application in Chemoenzymatic Synthesis". Angewandte Chemie International Edition. 50 (34): 7944–7947. doi:10.1002/anie.201008042. PMID 21744441. S2CID 42971817.
  • Studies on Diene-addition Reactions. II.1 The Reaction of 6,6-Pentamethylenefulvene with Maleic Anhydride R. B. Woodward, Harold Baer J. Am. Chem. Soc., 1944, 66 (4), pp 645–649 doi:10.1021/ja01232a042
  • Diels, O. and Alder, K. (1929), Synthesen in der hydroaromatischen Reihe, IV. Mitteilung: Über die Anlagerung von Maleinsäure-anhydrid an arylierte Diene, Triene und Fulvene (Mitbearbeitet von Paul Pries). Berichte der deutschen chemischen Gesellschaft (A and B Series), 62: 2081–2087. doi:10.1002/cber.19290620829
  • Rearrangement and substitution in anionotropic systems. Part III. Mechanism of, and equilibrium in, anionotropic change A. G. Catchpole, E. D. Hughes and C. K. Ingold J. Chem. Soc., 1948, 8-17 doi:10.1039/JR9480000008
  • Meisenheimer, J. and Link, J. (1930), Über die Verschiebung in der Allyl-Gruppe. 3. Mitteilung über Substitution und Addition. Justus Liebigs Annalen der Chemie, 479: 211–277. doi:10.1002/jlac.19304790114

nih.gov

pubmed.ncbi.nlm.nih.gov

pharmaxchange.info

rsc.org

pubs.rsc.org

  • Kseniya K. Borisova, Eugeniya V. Nikitina, Roman A. Novikov, Victor N. Khrustalev, Pavel V. Dorovatovskii, Yan V. Zubavichus, Maxim L. Kuznetsov, Vladimir P. Zaytsev, Alexey V. Varlamov and Fedor I. Zubkov. “Diels–Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control.” Chem. Commun., 2018, 54, pp 2850-2853. doi:10.1039/c7cc09466c http://pubs.rsc.org/en/content/articlelanding/2018/cc/c7cc09466c#!divAbstract

semanticscholar.org

api.semanticscholar.org

worldcat.org