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Pure Appl. Chem., 1991, Vol. 63, No. 2, pp. 213-221

http://dx.doi.org/10.1351/pac199163020213

Generation and study of enols and other reactive species

A. J. Kresge

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  • Kaweetirawatt Thanayuth, Yamaguchi Toru, Higashiyama Tsutomu, Sumimoto Michinori, Hori Kenji: Theoretical study of keto-enol tautomerism by quantum mechanical calculations (the QM/MC/FEP method). J. Phys. Org. Chem. 2012, 25, 1097. <http://dx.doi.org/10.1002/poc.2944>
  • Mandal Pulak Chandra, Das Suranjana, Mukhopadhyay Subrata: Mechanistic studies on the oxidation of glyoxylic and pyruvic acids by a {Mn3O4}4+ core in aqueous media. Int J Chem Kinet 2010, 42, 323. <http://dx.doi.org/10.1002/kin.20488>
  • Mandal Pulak Chandra, Bhattacharyya Jhimli, Das Suranjana, Mukhopadhyay Subrata, Kirschenbaum Louis J.: Mechanistic studies on the oxidation of pyruvic acid by an oxo-bridged diiron(III,III) complex in aqueous acidic media. J Polyhedron 2009, 28, 3162. <http://dx.doi.org/10.1016/j.poly.2009.07.009>
  • Cucinotta Clotilde S., Ruini Alice, Catellani Alessandra, Stirling András: Ab Initio Molecular Dynamics Study of the Keto–Enol Tautomerism of Acetone in Solution. Chem Eur J of Chem Phys 2006, 7, 1229. <http://dx.doi.org/10.1002/cphc.200600007>
  • Raczyńska Ewa D., Duczmal Kinga, Darowska Małgorzata: Experimental (FT-IR) and theoretical (DFT-IR) studies of keto–enol tautomerism in pyruvic acid. Vib Spect 2005, 39, 37. <http://dx.doi.org/10.1016/j.vibspec.2004.10.006>
  • Appoh Francis E., Sutherland Todd C., Kraatz Heinz-Bernhard: Changes in the hydrogen bonding pattern in ferrocene peptides. J Organomet Chem 2004, 689, 4669. <http://dx.doi.org/10.1016/j.jorganchem.2004.04.017>
  • Wang Daniel Ze-Rong, Streitwieser Andrew: Aggregation and ion pair acidity in THF: lithium and cesium enolates of α-phenylcyclohexanone. Can J Chem 1999, 77, 654. <http://dx.doi.org/10.1139/v99-025>
  • Hannon Christine L., Bell Dwayne A., Kelly-Rowley Anne M., Cabell Larry A., Anslyn Eric V.: NON-AQUEOUS TITRATIONS AS A TOOL IN THE STUDY OF MOLECULAR RECOGNITION PHENOMENA. USES IN DISTINGUISHING HYDROGEN BONDING FROM PROTON TRANSFER, THE MEASUREMENT OF COMPLEX INDUCED pKa SHIFTS, AND THE ABILITY TO DISTINGUISH THE CATALYTIC ROLES OF GENERAL ACIDS AND BASES. J Phys Org Chem 1997, 10, 396. <http://dx.doi.org/10.1002/(SICI)1099-1395(199705)10:5<396::AID-POC906>3.0.CO;2-S>
  • Ebbers Eelco J., Ariaans Gerry J.A., Houbiers Joannes P.M., Bruggink Alle, Zwanenburg Binne: Controlled racemization of optically active organic compounds: Prospects for asymmetric transformation. Tetrahedron 1997, 53, 9417. <http://dx.doi.org/10.1016/S0040-4020(97)00324-4>
  • Li Naixin, Rahil Jubrail, Wright Margaret E., Pratt R.F.: Structure-activity studies of the inhibition of serine β-lactamases by phosphonate monoesters. biorg med chem 1997, 5, 1783. <http://dx.doi.org/10.1016/S0968-0896(97)00103-X>
  • Perrin Charles L., Nielson Jennifer B.: “STRONG” HYDROGEN BONDS IN CHEMISTRY AND BIOLOGY. Ann Rev Phys Chem 1997, 48, 511. <http://dx.doi.org/10.1146/annurev.physchem.48.1.511>
  • Fenniri Hicham, Lehn Jean-Marie, Marquis-Rigault Annie: Supramolekulare Katalyse des H/D-Austausches in der α-Position bei Malonat-Ionen durch makrocyclische Polyamine: ein Modell-Enzym mit Enolase-Aktivität. Angew Chem 1996, 108, 337. <http://dx.doi.org/10.1002/ange.19961080315>
  • Binder Wolfgang H., Menger Fredric M.: Heptakis-6-amino-6-deoxy-β-cyclodextrin as a catalyst for H/D exchange. Tetrahetron Lett 1996, 37, 8963. <http://dx.doi.org/10.1016/S0040-4039(96)02103-X>
  • Korkin Anatoli, Mark Frank, Schaffner Kurt, Gorb Leonid, Leszczynski Jerzy, Jetton R.E., Nanney J.R., Mahaffy C.A.L., Sargent Andrew L., Rollog Mark E., Alml��f Jan E., Gassman Paul G., Gerlt John A.: Theoretical ab initio and semiempirical studies of biologically important di- and oligopyrrolic compounds: pyrromethene and protonated pyrromethene. Journal of Molecular Structure: THEOCHEM 1996, 388, 121. <http://dx.doi.org/10.1016/S0166-1280(96)80028-5>
  • Peter Guthrie J.: Short strong hydrogen bonds: can they explain enzymic catalysis?. CHEM BIOL 1996, 3, 163. <http://dx.doi.org/10.1016/S1074-5521(96)90258-6>
  • Shan S.-o., Herschlag D.: The change in hydrogen bond strength accompanying charge rearrangement: Implications for enzymatic catalysis. Proceedings of the National Academy of Sciences 1996, 93, 14474. <http://dx.doi.org/10.1073/pnas.93.25.14474>