| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271484 | Tetrahedron Letters | 2013 | 5 Pages |
Abstract
The Ugi-4C reaction employing Nβ-protected-amino alkyl isonitrile, amino acid ester, aldehyde, and glycosyl acid has resulted in novel glycosylated peptidomimetics. The extension of MCR products for the synthesis of N,Nâ²-orthogonally protected glycosylated peptidomimetics has also been demonstrated.
Graphical abstractUgi-4C reaction employing Nβ-protected-amino alkyl isonitrile, amino acid ester, aldehyde, and glycosyl acid has resulted in novel glycosylated peptidomimetics. Further, the protocol has been extended for the synthesis of N,Nâ²-orthogonally protected glycosylated peptidomimetics as well.Download full-size image
Related Topics
Physical Sciences and Engineering
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Authors
Basavalingappa Vasantha, Girish Prabhu, Hosmani Basavaprabhu, Vommina V. Sureshbabu,