An efficient reduction of acetals and ketals to methyl ethers.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Reduction with Metal Hydrides. XII. Reduction of Acetals and Ketals with Lithium Aluminum Hydride-Aluminum Chloride
2. Pentaerythritol Derivatives. V.1 Preparation of Diethers of Pentaerythritol by Reduction of Acetals and Ketals2
3. Hydrogenolysis of Ketals
4. Reductive Cleavage of Acetals and Ketals by Borane
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2. Regioselective Ring Opening of 1,3-Dioxane-Type Acetals in Carbohydrates;European Journal of Organic Chemistry;2018-11-27
3. Sodium Cyanoborohydride;Encyclopedia of Reagents for Organic Synthesis;2016-12-01
4. Oxidative and reductive ring opening of endo-3,4-O-(4-methoxybenzylidene) acetals of 1, 6-anhydro-β-D-galactopyranoses;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
5. Sodium Cyanoborohydride;Encyclopedia of Reagents for Organic Synthesis;2007-03-15
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