| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278945 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Pyrazolo-pyranosides prepared from methyl-2,3:4,6-di-O-benzylidene-α-d-mannopyranoside were functionalized to design new scaffolds suitable for peptidomimetic construction. Under certain acidic conditions, they undergo only pyranose ring-opening generating highly functionalized optically pure pyrazoles bearing an aldehyde function.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Issa Samb, Nadia Pellegrini-Moïse, Yves Chapleur,