Chiral discrimination in cycloaddition experiments
Literature Information
Publication Date
DOI
10.1039/CC9960000887
Impact Factor
6.222
Authors
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Abstract
Various applications of a chiral cyclopentadiene in chiral recognition experiments are reported. Racemic cyclic dienophiles undergo very efficient kinetic resolution while with prochiral cyclohexadienones discrimination of enantiotopic groups is observed. In one particular case a racemic exo-methylene lactone from to a highly stereospecific cycloaddition yielded to topographic resolution.
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Source Journal
Chemical Communications
CiteScore:
8.6
Self-citation Rate:
4.7%
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2458
ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry
Recommended Compounds
![N-[2-(4-Hydroxyphenoxy)-4-nitrophenyl]methanesulfonamide structure](https://static.chemtradehub.com/structs/109/109032-22-6-7c88.webp "N-[2-(4-Hydroxyphenoxy)-4-nitrophenyl]methanesulfonamide structure")
N-[2-(4-Hydroxyphenoxy)-4-nitrophenyl]methanesulfonamide
CAS Number:
109032-22-6
Molecular Formula:
C13H12N2O6S
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