Asymmetric induction in mixed [2 + 2] photoadditions employing a chiral auxiliary in the alkene component
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. The use of chiral solvating agent for nuclear magnetic resonance determination of enantiomeric purity and absolute configuration of lactones. Consequences of three-point interactions
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3. Nuclear magnetic resonance determination of enantiomeric composition and absolute configuration of .gamma.-lactones using chiral 2,2,2-trifluoro-1-(9-anthryl)ethanol
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1. Enantiodifferentiating [2+2] photocycloaddition of cyclohexenone carboxylic acid with ethylene using 8-phenylmenthyl amine as a chiral template;Tetrahedron Letters;2014-03
2. Diastereoselective [2 + 2] Photocycloaddition of Cyclohexenone Derivative with Olefins in Supercritical Carbon Dioxide;The Journal of Organic Chemistry;2013-07-11
3. Highly diastereodifferentiating and regioselective [2+2]-photoreactions using methoxyaromatic menthyl cyclohexenone carboxylates;Tetrahedron;2013-01
4. Photochemistry of Compounds Containing CC Double Bonds;PATAI'S Chemistry of Functional Groups;2009-12-15
5. Asymmetric Total Synthesis of (−)-Linderol A;The Journal of Organic Chemistry;2007-06-19
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