Diels-alder reactions with 2,2-bis(trifluoromethyl)-ethylene-1,1-dicarbonitrile as dienophile
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Tetracyanoethylene and enol ethers. A model for 2 + 2 cycloadditions via zwitterionic intermediates
2. Can tetramethylene intermediates be intercepted?
3. Kinetics of [2+2] cycloadditions of 2,2-bis(trifluoromethylethylene-1,1-dicarbonitrile with enol ethers, 1,1-dimethylbutadiene, and allyltrimethylsilane
4. [2 + 2] cycloadditions of 2,2-bis(trifluoromethyl)ethylene-1,1-dicarbonitrile with vinyl sulfides and ketene S,S-acetals
5. 1,1-Dicyano-2,2-bis(trifluoromethyl)ethylene1
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1. ChemInform Abstract: Diels-Alder Reactions with 2,2-Bis(trifluoromethyl)ethylene-1,1- dicarbonitrile as Dienophile.;ChemInform;2010-08-19
2. Fluorinated Cyclobutanes and Their Derivatives;PATAI'S Chemistry of Functional Groups;2009-12-15
3. Synthesis of Cyclobutanes;PATAI'S Chemistry of Functional Groups;2009-12-15
4. Reactions of 2-Unsubstituted 1H-Imidazole 3-Oxides with 2,2-Bis(trifluoromethyl)ethene-1,1-dicarbonitrile: A Stepwise 1,3-Dipolar Cycloaddition;Helvetica Chimica Acta;2006-07
5. Photocycloaddition of cyclohex-2-enones to alkylidenemalononitriles (1,1-dicyanoalkenes);Photochemical & Photobiological Sciences;2005
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