HClO4-SiO2 catalyzed chemoselective synthesis of acylals from aldehydes under solvent-free conditions
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Process Chemistry and Technology,Catalysis
Reference19 articles.
1. Protective Groups in Organic Synthesis;Greene,1999
2. The Chemistry of Acylals. 3. Cyanohydrin Esters from Acylals with Cyanide Reagents
3. gem-Diacetates as Carbonyl Surrogates for Asymmetric Synthesis. Total Syntheses of Sphingofungins E and F
4. Asymmetric Alkylation of Allylic gem-Dicarboxylates
5. Diels–Alder route to potential trichothecene precursors
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1. Supported N-propylsulfamic acid onto Fe3O4 magnetic nanoparticles as a reusable and efficient nanocatalyst for the protection/deprotection of hydroxyl groups and protection of aldehydes;Research on Chemical Intermediates;2015-08-29
2. Nano-Fe3O4-encapsulated silica particles bearing sulfonic acid groups as a magnetically separable catalyst for green synthesis of 1,1-diacetates;Green Chemistry Letters and Reviews;2014-01-02
3. Chemoselective Synthesis of 1,1-Diacetate from Aldehydes Catalyzed by Sulfonated Carbon Nanocage;CHEM J CHINESE U;2013
4. NaHSO4-SiO2 as an efficient and chemoselective catalyst, for the synthesis of acylal from aldehydes under, solvent-free conditions;Chemistry Central Journal;2012-11-13
5. Solvent-free catalytic preparation of 1,1-diacetates using a silica-supported functional ionic liquid as catalyst;Monatshefte für Chemie - Chemical Monthly;2012-05-22
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