Quantitative structure-activity relationships for the enantioselectivity of oxirane ring-opening catalyzed by epoxide hydrolases

…, T Suzuki, JA Paier, A Steinreiber, K Faber…

Index: Kroutil, Wolfgang; Osprian, Ingrid; Mischitz, Martin; Faber, Kurt Synthesis, 1997 , # 2 p. 156 - 158

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Citation Number: 20

Abstract

The enantioselective ring-opening catalyzed by epoxide hydrolases originating from seven different sources of a series of 2, 2-disubstituted oxiranes containing alkyl chains of different lengths, unsaturated (alkenyl, alkinyl) and aromatic groups as well as electronegative

Synthèse efficace des méthyl-2 hexanediols-1, 2 optiquement actifs

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A method for the extraction of chlorophyll from leaf tissue without maceration

[Yadav, J. S.; Satyanarayana Reddy, P.; Jolly, R. S. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1986 , vol. 25, p. 294 - 295]

Chemoenzymatic deracemization of (±)-2, 2-disubstituted oxiranes

[Orru, Romano V. A.; Mayer, Sandra F.; Kroutil, Wolfgang; Faber, Kurt Tetrahedron, 1998 , vol. 54, # 5-6 p. 859 - 874]