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Solid phase synthesis of heterocyclic compounds from linear peptides: Cyclic ureas and thioureas
β Scribed by Adel Nefzi; John M. Ostresh; Jean-Philippe Meyer; Richard A. Houghten
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 207 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The solid phase synthesis of cyclic ureas and thioureas is described. The reduction of acylated dipeptides followed by treatment with carbonyldiimidazole or thiocarbonyldiimidazole affords the corresponding cyclic urea or thiourea in good yield and high purity. This is an example of a broader approach to the solid phase synthesis of individual heterecyclic compounds and combinatorial libraries using peptides as starting materials.
π SIMILAR VOLUMES
We synthesized a 18 residues cyclic ppcicle correqonding to a loop involved in tk cumremimetic action of a snake toxic pmtein. This peptide. whii ccnn~les with Ihe native toxin for the binding lo the nicolinic ucetylcholii mzeptor, inclti the Bturn inducing Pro-AW moiety. Gibe peptide wax pqxued and