Synthesims of 7-oxabicyclo[2.2.1]heptanes and 8-oxabicyclo[3.2.1]octanes from C-glycosides via an intramolecular cyclization

From National Research Council Canada

DOIResolve DOI: https://doi.org/10.1021/jo3024973
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Affiliation
  1. National Research Council of Canada. NRC Institute for Biological Sciences
FormatText, Article
SubjectAnomeric configuration; C-glycosides; Chemical yields; Enamine intermediates; Epimerization; Intramolecular cyclizations; Nucleophilic substitutions; Pyrrolidines; Cyclization; Heptane; Stereoselectivity; Sugars; 7 oxabicyclo [2 2 1] heptane; 8 oxabicyclo [3 2 1]octane; glycoside; heptane; octane; pyrrolidine derivative; unclassified drug; bicyclo compound; C glycoside; C-glycoside; cycloheptane derivative; cyclooctane derivative; monosaccharide; chemical reaction; chemical structure; cyclization; epimerization; nucleophilicity; stereochemistry; synthesis; chemistry; cyclization; stereoisomerism; Bicyclo Compounds; Cyclization; Cycloheptanes; Cyclooctanes; Molecular Structure; Monosaccharides; Stereoisomerism
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LanguageEnglish
Peer reviewedYes
NPARC number21269925
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Record created2013-12-13
Record modified2020-04-22
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