The dichlorovinylation of enolates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. A nickel catalyst for the arylation and vinylation of lithium ester enolates
2. Regiospecific alkylation of cyclic .beta.-diketone enol ethers. General synthesis of 4-alkylcyclohexenones
3. Empirical Method for Estimating Diamagnetic Anisotropy Effects in NMR Spectroscopy, Based upon the Use of C13–H Coupling Constants
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1. Silver catalyzed proto- and sila-Nakamura-type α-vinylation of silyl enol ethers with dichloroacetylene. Divergent formation of stereochemically pure tri- and tetrasubstituted olefins;Tetrahedron Letters;2020-01
2. Dichloroenol Ethers X-ray Analysis in the Mechanistic Elucidation of Ynol Ethers Formation;Journal of Chemical Crystallography;2011-03-23
3. Ethynyl-1,2-benziodoxol-3(1 H)-one (EBX): An Exceptional Reagent for the Ethynylation of Keto, Cyano, and Nitro Esters;Chemistry - A European Journal;2010-07-19
4. Multiple hydride reduction pathways in isoflavonoids;Beilstein Journal of Organic Chemistry;2006-08-25
5. Vinylation of Enolates with a Vinyl Cation Equivalent:trans-3-Methyl-2-Vinylcyclohexanone;Organic Syntheses;2003-04-28
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