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A coherent study on the: Z -enoate assisted Meyer-Schuster rearrangement
, Tharra P.
Published in Royal Society of Chemistry
2017
Volume: 15
   
Issue: 26
Pages: 5579 - 5584
Abstract
A systematic study has been performed on the Z-enoate assisted Meyer-Schuster rearrangement of propargylic alcohols. The impact of various factors such as temperature, solvent, concentration of a counter ion of an acid, and the nature of the arene nucleophile was studied. The relative nucleophilicity of various arenes estimated in this study is in good agreement with that of Herbert Mayr's nucleophilicity scale. © 2017 The Royal Society of Chemistry.
About the journal
JournalData powered by TypesetOrganic and Biomolecular Chemistry
PublisherData powered by TypesetRoyal Society of Chemistry
ISSN14770520
Open AccessNo