P2O5/SiO2as an Efficient Reagent for Selective Deprotection of 1,1-Diacetates under Solvent-Free Conditions
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jccs.200500024/fullpdf
Reference37 articles.
1. Protective Groups in Organic Synthesis
2. Simple Protocol for Synthesis and Cleavage of Tetrahydropyranyl Ethers Using FeSO4as an Inexpensive Catalyst
3. Remarkably Fast Deprotection of Semicarbazones and Tosylhydrazones Under Mild, Neutral and Solvent-Free Conditions
4. An Efficient and Highly Chemoselective Method to Desilylate Silyl Ethers
5. Protecting groups in organic synthesis. Part 8. Conversion of aldehydes into geminal diacetates
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1. Zinc zirconium phosphate as an efficient catalyst for chemoselective synthesis of 1,1-diacetates under solvent-free conditions;Journal of Chemical Sciences;2015-11
2. Solvent-free Chemoselective Synthesis of 1,1-diacetates Catalyzed by Iron Zirconium Phosphate;Journal of the Chinese Chemical Society;2015-10-08
3. Solvent-free Preparation of 5-Aryloxytetrazoles via [2+3] Cycloaddition of Cyanates and Sodium Azide Using Silica Supported Sulfuric Acid as an Effective Heterogeneous Catalyst;Chemistry of Heterocyclic Compounds;2014-01
4. P2O5/SiO2 as an efficient heterogeneous catalyst for the synthesis of heterocyclic alkene derivatives under thermal solvent-free conditions;Catalysis Science & Technology;2013
5. Phosphorus pentoxide supported on silica gel and alumina (P2O5/SiO2, P2O5/Al2O3) as useful catalysts in organic synthesis;Journal of the Iranian Chemical Society;2012-01-13
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