Highly diastereoselective radical reactions of substituted methylideneimidazolidinones and related systems
Date
2004
Authors
Adamson, George
Beckwith, Athelstan (Athel)
Chai, Christina
Journal Title
Journal ISSN
Volume Title
Publisher
CSIRO Publishing
Abstract
Stannane-mediated radical addition to tnethylideneimidazolidinones occurs with good to excellent diastereo-selectivity. The stereochemical outcome of addition is highly dependent on the nature of the NI substituent on the imidazolidinone ring.
Description
Keywords
Keywords: Amino acids; Chemical bonds; Free radical reactions; Free radicals; Photolysis; Stereochemistry; Structure (composition); Substitution reactions; Substrates; Diastereoselectivity; Enantioselectivity; Regioselectivity; Aromatic compounds
Citation
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Source
Australian Journal of Chemistry
Type
Journal article