Donor-substituted furans and 1,2-bis(trifluoromethyl)ethylene-1,2-dicarbonitrile: A novel rearrangement and its steric course
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Orbital energy control of cycloaddition reactivity
2. Ionization potentials, electron affinities, and reactivities of cyanoalkenes and related electron-deficient alkenes. A frontier molecular orbital treatment of cyanoalkene reactivities in cycloaddition, electrophilic, nucleophilic, and radical reactions
3. Stereochemistry of the Cycloaddition Reaction of 1,2-Bis(trifluoromethyl)-1,2-dicyanoethylene and Electron-Rich Alkenes1
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1. Cyclopropanation of (E)-Dehydroaspartic Acid Esters with Furan Derivatives: The Synthesis of Highly Functionalized α-2,3-Methanoamino Acid Esters;Synlett;2015-06-18
2. Ring Opening of Donor-Substituted Furans by Dimethyl 2,3-Dicyanofumarate;Bulletin des Sociétés Chimiques Belges;2010-09-01
3. ChemInform Abstract: Donor-Substituted Furans and 1,2-Bis(trifluoromethyl)ethylene-1,2- dicarbonitrile: A Novel Rearrangement and Its Steric Course.;ChemInform;2010-08-18
4. Synthesis of fluorofurans and perfluoroalkylfurans;Journal of Fluorine Chemistry;2010-03
5. Novel formation of phenylcyclopropanes from the reaction of β-cyanostyrenes and related compounds with 2-methoxyfuran: experimental and theoretical studies;New Journal of Chemistry;2009
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