Preparation of Geminal Diacylates (Acylals) of Aldehydes – Scope and Reactivity of Aldehydes with Acid Anhydrides
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference59 articles.
1. , Protective Groups in Organic Synthesis, 3rd ed., John Wiley & Sons, New York, 1999 , p. 306.
2. Protecting groups in organic synthesis. Part 8. Conversion of aldehydes into geminal diacetates
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4. Alumina-mediated deacetylation of benzaldehyde diacetates. A simple deprotection method
5. TiO2/SO42-: A Facile and Efficient Catalyst for Deprotection of 1,1-diacetates
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1. Formyloxyacetoxyphenylmethane and 1,1-diacylals as versatile O-formylating and O-acylating reagents for alcohols;Tetrahedron;2018-11
2. 1,1-Diacyloxy-1-phenylmethanes as versatile N-acylating agents for amines;Tetrahedron;2018-09
3. Zinc zirconium phosphate as an efficient catalyst for chemoselective synthesis of 1,1-diacetates under solvent-free conditions;Journal of Chemical Sciences;2015-11
4. Chemoselective Synthesis of 1,1-Diacetate from Aldehydes Catalyzed by Sulfonated Carbon Nanocage;CHEM J CHINESE U;2013
5. Mild and Chemoselective Synthesis and Deprotection of Geminal Diacetates Catalyzed by Titanium(IV) Halides;Synthesis;2010-06-25
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