Enantioselective photodeconjugation of α,β-unsaturated esters in the presence of catalytic amounts of a chiral-inducing entity
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. .beta.,.gamma.-unsaturated acids and esters by photochemical isomerization of .alpha.,.beta.-congeners
2. A Study on the Photochemistry of α,β-Unsaturated γ-Lactones. II. Photoisomerization of 3-Ethylidene-4,5-dihydro-2(3H)-furanone
3. A Convenient Synthesis of α-Vinyl-lactones by Photo-Deconjugation of α,β-Unsaturated γ- or δ-Lactones
4. Conversion of .alpha.,.beta.-unsaturated esters to their .beta.,.gamma.-unsaturated isomers by photochemical deconjugation
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1. Asymmetric Protonation of Carbanions and Polar Double Bonds: Application to Total Syntheses;Stereoselective Synthesis of Drugs and Natural Products;2013-10-02
2. Organocatalyzed Enantioselective Protonation;Enantioselective Organocatalyzed Reactions I;2011
3. Asymmetric Photoreactions of Conjugated Enones and Esters;Advances in Photochemistry;2007-01-05
4. Enantioselective protonations: fundamental insights and new concepts;Tetrahedron: Asymmetry;2004-11
5. Photodeconjugation of Enones and Carboxylic Acid Derivatives;CRC Handbookof Organic Photochemistry and Photobiology, Volumes 1 & 2, Second Edition;2003-09-29
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