Enzymatic kinetic separation of stereoisomeric macrocyclic lactone derivatives, 7α,β-O-acyl trans-zearalenols and 7α,β-O-acyl zearanols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Total Synthesis of (−)-Zearalenone and (−)-Zearalanone: A Macrocyclization Strategy by Ni/Zr/Cr-Mediated Reductive Ketone Coupling;The Journal of Organic Chemistry;2024-09-10
2. ChemInform Abstract: Enzymatic Kinetic Separation of Stereoisomeric Macrocyclic Lactone Derivatives, 7α,β-O-Acyl trans-Zearalenols and 7α,. beta.-O-Acyl Zearanols.;ChemInform;2010-08-21
3. Kinetic resolution of diastereomeric racemates of 7-bromo-3-(1′-hydroxyethyl)-1-methyl-5-(2′-pyridyl)-2,3-dihydro-1H-1,4-benzodiazepin-2-one by immobilized CAL-B;Tetrahedron: Asymmetry;2003-09
4. Complex of Burkholderia cepacia lipase with transition state analogue of 1-phenoxy-2-acetoxybutane;European Journal of Biochemistry;2001-07-15
5. Comparative study of conformational effects on stereoselective lipase catalysed acetylation of sec hydroxy groups in diastereomeric 14-membered lactones and their acyclic analogs;Tetrahedron Letters;2000-11
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