Preparation of isobutyl 3,4-anhydro-2, 6-dideoxy-DL-α-lyxo--hexopyranoside and its kinetic resolution with microsomal epoxide hydrolase-Reference-Cited by-同舟云学术

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Preparation of isobutyl 3,4-anhydro-2, 6-dideoxy-DL-α-lyxo--hexopyranoside and its kinetic resolution with microsomal epoxide hydrolase

Published:1989-01 Issue:5 Volume:45 Page:1553-1566
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Barili Pier Luigi,Berti Giancarlo,Catelani Giorgio,Colonna Fabrizia,Mastrorilli Ettore,Paoli Marco

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference20 articles.

1. Alkaline and enzymatic hydrolysis of isobutyl 3,4-anhydro-2,6-dideoxy-DL-hexopyranosides. Preparation of enantiomeric boivinopyranosides through a highly efficient kinetic resolution

2. Alkaline hydrolysis of methanesulfonate esters without inversion

Cited by 3 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. Reactions of alicyclic epoxy compounds with oxygen-centered nucleophiles;Russian Journal of Organic Chemistry;2006-03

2. Regio- and stereochemistry of the acid catalyzed and of a highly enantioselective enzymatic hydrolysis of some epoxytetrahydrofurans.;Tetrahedron;1993-07

3. ChemInform Abstract: Preparation of Isobutyl 3,4-Anhydro-2,6-dideoxy-DL-α-lyxo-hexopyranoside and Its Kinetic Resolution with Microsomal Epoxide Hydrolase.;ChemInform;1989-07-11

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