α-(Benzotriazolyl)methyl phenyl thioethers: Convenient reagents for α-phenylthioalkylation of silylated nucleophiles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. The synthesis of α-acetoxy sulfides and their lewis acid-mediated reactions
2. α-methylenation of lactones and esters zinc bromide-catalysed phenylthiomethylation of o-silylated enolates
3. Regiospecific α-methylenation and α-methylation of ketones: titanium tetrachloride promoted phenylthiomethylation of silyl enol ethers
4. α-Alkylation and α-alkylidenation of carbonyl compounds: Lewis acid-promoted phenylthioalkylation of o-silylated enolates
5. O-silylated enolate phenylthioalkylation: a new synthesis of unsaturated 1,5-dicarbonyl compounds.
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1. First Zinc Bromide Promoted Annulative Domino Reactions between Enamines and Cyclic Morita–Baylis–Hillman Alcohols: Synthesis of N,O-Ketals;Synlett;2020-04-06
2. Direct palladium-catalyzed allylic alkylations of alcohols with enamines: Synthesis of homoallyl ketones;Tetrahedron Letters;2017-06
3. Palladium-catalyzed nucleophilic allylic substitution of Morita–Baylis–Hillman adducts with enamines: Synthesis of 1,5-dicarbonyl compounds;Comptes Rendus Chimie;2017-05
4. 4.1.3.3. Organocatalytic Enantioselective Michael Addition of Thiophenol to Chalcone;Comprehensive Organic Chemistry Experiments for the Laboratory Classroom;2016-12-16
5. ChemInform Abstract: α-(Benzotriazolyl)methyl Phenyl Thioethers: Convenient Reagents for α-Phenylthioalkylation of Silylated Nucleophiles.;ChemInform;2010-08-04
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