α-Alkylation of ketones, esters, and lactones: zinc bromide-catalysed alkylation of o-silylated enolates, a synthesis of (±)-ar-turmerone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. α-t-Butylation of aldehydes and ketones by the Friedel-Crafts alkylation of trimethylsilyl enol ethers
2. tert-Alkylation of Ketones and Aldehydes
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4. Reaction of lithium N-isopropylcyclohexylamide with esters. Method for the formation and alkylation of ester enolates
5. A New Method for the Alkylation of Ketones and Aldehydes: the C-Alkylation of the Magnesium Salts of N-Substituted Imines
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2. Zinc bromide: a general mediator for the ionothermal synthesis of microporous polymers via cyclotrimerization reactions;Journal of Materials Chemistry A;2023
3. Organosilicon Reducing Reagents for Stereoselective Formations of Silyl Enol Ethers from α-Halo Carbonyl Compounds;The Journal of Organic Chemistry;2018-01-29
4. Stereoselective Alkylation of the Vinylketene Silyl N,O-Acetal and Its Application to the Synthesis of Mycocerosic Acid;Organic Letters;2015-12-16
5. 3.01 Alkylations of Enols and Enolates;Comprehensive Organic Synthesis II;2014
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