Lithium perchlorate catalyzed conjugate addition of o-silylated ketene acetals to hindered α,β-unsaturated carbonyl compounds at atmospheric pressure
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. O-silylated ketene acetal chemistry; β-(alkoxycarbonyl)methyl O-silyl enolates, useful synthons for α-substituted-β-(alkoxycarbonyl)methylalkanones
2. THE MICHAEL TYPE REACTION OF O-SILYLATED KETENE ACETALS WITH α,β-UNSATURATED CARBONYL COMPOUNDS PROMOTED BY TITANIUM TETRACHLORIDE
3. Total synthesis of dl-quadrone
4. The Highly Stereoselective Michael Reaction of α,β-Unsaturated Ketones with Silyl Enol Ethers of Thioesters Catalyzed by Trityl Salts. A Facile Stereoselective Synthesis of 5-Oxocarboxylic Acid Ester Derivatives
5. Activation of ketene silyl acetals by 10-methylacridinium perchlorate: a novel catalysis in mukaiyama reaction
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