An Efficient and Practical Procedure for Preparation of Gem-Diacetates from Aldehydes Catalysed by Magnesium Perchlorate
Author:
Affiliation:
1. The College of Chemistry & Material Science, Hebei Normal University, Shijiazhuang 050016, P. R. China
Abstract
Publisher
SAGE Publications
Subject
General Chemistry
Link
http://journals.sagepub.com/doi/pdf/10.3184/030823406776330648
Reference60 articles.
1. Reinvestigation of the Mechanism ofgem-Diacylation: Chemoselective Conversion of Aldehydes to Variousgem-Diacylates and Their Cleavage under Acidic and Basic Conditions
2. Protecting groups in organic synthesis. Part 8. Conversion of aldehydes into geminal diacetates
3. Montmorillonite clay catalysis V1: An efficient and facile procedure for deprotection of 1,1-diacetates
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1. Perchloric Acid and Its Salts: Very Powerful Catalysts in Organic Chemistry;Chemical Reviews;2010-03-17
2. 1,3-Dibromo-5,5-dimethylhydantoin or N-bromosuccinimide as efficient reagents for chemoselective deprotection of 1,1-diacetates under solvent-free conditions;Monatshefte für Chemie - Chemical Monthly;2009-11-07
3. Silica-supported antimony(III) chloride as an efficient heterogeneous catalyst for the synthesis of aminopropenones and 3-aminopropenoates under solvent-free conditions;Russian Journal of Organic Chemistry;2009-01
4. A stable intermediate: a new insight into the mechanism of Lewis acids-promoted formation of acylals from aldehydes;Tetrahedron Letters;2007-04
5. A Facile and Efficient Conversion of Aldehydes into 1,1-Diacetates (Acylals) using Iron(III) Fluoride as a Novel Catalyst;Australian Journal of Chemistry;2007
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