Enzyme-catalysed esterification of (±)-trans-cyclohexane-1,2-dimethanol
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference10 articles.
1. An efficient synthesis of both enantiomers of trans-1,2-cyclopentanediol and their conversion to two novel bidentate phosphite and fluorophosphinite ligands
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. ChemInform Abstract: Enzyme-Catalyzed Esterification of (.+-.)-trans-Cyclohexane-1,2- dimethanol.;ChemInform;2010-08-20
2. Regioselective resolution of 1,n-diols catalysed by lipases: a rational explanation of the enzymayic selectivity;Journal of Molecular Catalysis B: Enzymatic;2001-01
3. Acyclic phenylalkanediols as substrates for the study of enzyme recognition. Regioselective acylation by porcine pancreatic lipase: a structural hypothesis for the enzymatic selectivity;Tetrahedron;1999-12
4. A computer program for analysis, simulation and optimization of asymmetric catalytic processes proceeding through two consecutive steps. Type 2: sequential kinetic resolutions;Tetrahedron: Asymmetry;1997-10
5. Synthesis of Enantiomerically Pure Bis(hydroxymethyl)-Branched Cyclohexenyl and Cyclohexyl Purines as Potential Inhibitors of HIV;The Journal of Organic Chemistry;1996-01-01
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