Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1966, 31, 2615-2618
https://doi.org/10.1135/cccc19662615

Asymmetric reactions. XI. Sterical course of enzymatic reduction of methyl alkyl ketones and methyl aryl ketones

O. Červinka and L. Hub

Crossref Cited-by Linking

  • Saxon Rachel E., Leisch Hannes, Hudlicky Tomas: Preliminary investigation of the yeast-mediated reduction of β-keto amides derived from cyclic amines as potential resolution methodology. Tetrahedron: Asymmetry 2008, 19, 672. <https://doi.org/10.1016/j.tetasy.2008.02.021>
  • Martínez-Lagos F., Sinisterra J.V.: Enantioselective production of halohydrin precursor of Propranolol catalysed by immobilized yeasts. Journal of Molecular Catalysis B: Enzymatic 2005, 36, 1. <https://doi.org/10.1016/j.molcatb.2005.06.012>
  • Martı́nez Lagos Fernando, Carballeira Jose D., Bermúdez Jose L., Alvarez Emilio, Sinisterra Jose V.: Highly stereoselective reduction of haloketones using three new yeasts: application to the synthesis of (S)-adrenergic β-blockers related to propranolol. Tetrahedron: Asymmetry 2004, 15, 763. <https://doi.org/10.1016/j.tetasy.2004.01.024>
  • Yadav J. S., Nanda S., Reddy P. Thirupathi, Rao A. Bhaskar: Efficient Enantioselective Reduction of Ketones with Daucus carota Root. J. Org. Chem. 2002, 67, 3900. <https://doi.org/10.1021/jo010399p>
  • Odinokov V. N., Botsman L. P., Saranova L. V., Syutkina E. V., Emel'yanova G. A.: Insect pheromones and their analogs LVI. Chemical-enzymatic synthesis of (S)-(+)-9-hydroxydec-2E-enoic acid, a component of the queen pheromone of the honeybeeApis mellifera. Chem Nat Compd 1997, 33, 687. <https://doi.org/10.1007/BF02249642>
  • Naemura Koichiro, Murata Masaki, Tanaka Rie, Yano Masashi, Hirose Keiji, Tobe Yoshito: Enantioselective acylation of primary and secondary alcohols catalyzed by lipase QL from Alcaligenes sp.: A predictive active site model for lipase QL to identify which enantiomer of an alcohol reacts faster in this acylation. Tetrahedron: Asymmetry 1996, 7, 3285. <https://doi.org/10.1016/0957-4166(96)00429-6>
  • Kawai Yasushi, Hida Kouichi, Nakamura Kaoru, Ohno Atsuyoshi: Introduction of plural asymmetric centers by a β-keto ester reductase from baker's yeast. Tetrahedron Letters 1995, 36, 591. <https://doi.org/10.1016/0040-4039(94)02260-I>
  • Naemura Koichiro, Fukuda Ritsuko, Murata Masaki, Konishi Masayoshi, Hirose Keiji, Tobe Yoshito: Lipase-catalyzed enantioselective acylation of alcohols: a predictive active site model for lipase YS to identify which enantiomer of an alcohol reacts faster in this acylation. Tetrahedron: Asymmetry 1995, 6, 2385. <https://doi.org/10.1016/0957-4166(95)00316-H>
  • Spassov G., Pramatarova V., Vlahov R., Snatzke G.: Stereoselective reduction of substituted benzophenones by microorganisms I. Tetrahedron: Asymmetry 1993, 4, 301. <https://doi.org/10.1016/S0957-4166(00)86073-5>
  • Tkachev Alexey V., Rukavishnikov Alexey V., Gatilov Yuri V., Bagrjanskaja Irina Yu.: Baker's yeast-induced asymmetric reduction of the keto group activated by the cyclopropane unit. Tetrahedron: Asymmetry 1992, 3, 1165. <https://doi.org/10.1016/S0957-4166(00)82103-5>
  • Gillois Jeannine, Jaouen Gérard, Buisson Didier, Azerad Robert: Synthèse asymétrique d'alcools benchrotréniques par voie microbiologique. Journal of Organometallic Chemistry 1989, 367, 85. <https://doi.org/10.1016/0022-328X(89)87209-2>
  • Lis Randall, Caldwell Walton B., Rudd Gregory I., Lumma William C., Hoyer Georg Alexander, Petzoldt Karl, Cleve Gerhard, Sauer Gerhard: Product stereospecificity in the microbial reduction of imidazol-1-yl methyl aryl ketones. Tetrahedron Letters 1987, 28, 1487. <https://doi.org/10.1016/S0040-4039(01)81022-4>
  • Eichberger G�nter, Faber Kurt, Griengl Herfried: Reduktion 4-substituierter Acetophenone mittels Hefe. Monatsh Chem 1985, 116, 1233. <https://doi.org/10.1007/BF00811257>
  • Sih Charles J., Chen Ching-Shih: Mikrobielle asymmetrische Katalyse — enantioselektive Reduktion von Ketonen. Angew. Chem. 1984, 96, 556. <https://doi.org/10.1002/ange.19840960806>
  • Sih Charles J., Chen Ching‐Shih: Microbial Asymmetric Catalysis—Enantioselective Reduction of Ketones [New Synthetic Methods (45)]. Angew. Chem. Int. Ed. Engl. 1984, 23, 570. <https://doi.org/10.1002/anie.198405701>
  • Methyl isopropyl ketone. Food and Cosmetics Toxicology 1978, 16, 819. <https://doi.org/10.1016/S0015-6264(78)80131-X>
  • Lombardo Anthony, Dittmer Donald C.: Specificity in addition of a halomethyl group to a model for a pyridine nucleotide coenzyme. Bioorganic Chemistry 1971, 1, 400. <https://doi.org/10.1016/0045-2068(71)90042-3>