| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5222293 | Tetrahedron | 2009 | 5 Pages |
Abstract
1,2-Cyclic sulfite xylosides offer facile access to 1,2-oxazolines upon reaction with aromatic and alkyl nitriles under Lewis or Brönsted acid conditions. Additionally, hydrophobic ionic liquids facilitate acid-catalysed formations of such oxazolines and C- and O-linked xylosides, providing means to carry out fast reactions at room temperature, and this in yields comparable to reactions conducted in xylene at high temperature for extended reaction time.
Graphical abstractDownload full-size image
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Nathalie Batoux, Christopher Hardacre, Marie E. Migaud, Kerry A. Ness, Sarah E. Norman,