The chemical ligation of selectively S-acylated cysteinepeptides to form native peptides via 5-, 11- and 14-membered cyclic transition states

Faculty Pharmacy Year: 2010
Type of Publication: ZU Hosted Pages: 2316-2319
Authors:
Zakareyah Kamel Abdelsamie
Journal: Org. Biomol. Chem Org. Biomol. Chem Volume: 1
Keywords : , chemical ligation , selectively S-acylated cysteinepeptides , form    
Abstract:
The chemical ligation of selectively S-acylated cysteinepeptides to form native peptides via 5-, 11- and 14-membered cyclic transition states
    
     
 
       

Author Related Publications

  • Zakareyah Kamel Abdelsamie, "Regioselective hydroxysulphenylation of derivatives of allylic alcohols and amines.", Tetrahedron Letters, 1986 More
  • Zakareyah Kamel Abdelsamie, "New routes to heterocycles via sulphenylation of unsaturated amides", Tetrahedron Letters, 1987 More
  • Zakareyah Kamel Abdelsamie, "Trifluoroacetoxysulphenylation of unsaturated nitriles as a route to lactones", Tetrahedron Letters, 1986 More
  • Zakareyah Kamel Abdelsamie, "Synthesis of certain s-triazolo[3,4-b]-1,3,4-thiadiazole derivatives of pharmaceutical interest", Eygpt J. Pharm. Sci, 1987 More
  • Zakareyah Kamel Abdelsamie, "Synthesis and biological activity of some novel triazolothiadiazines", Eygpt J. Pharm. Sci, 1988 More

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  • Hanan Abdelraziek Abdelfattah Ali Hamied, "Synthesis of some imidazole Derivatives with Potential Biological Activityl", لايوجد, 1900 More
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