Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yousra Hamdane"'
Publikováno v:
Synthesis. 54:1518-1526
N-Amino-imidazol-2-one (Nai) residues are tools for studying peptide-backbone and side-chain conformation and function. Recent methods for substituted Nai residue synthesis, conformational analysis by X-ray crystallography and computation, and biomed
Autor:
Yousra Hamdane, Suresh Vutla, Pradeep S. Chauhan, Mukandila Mulumba, William D. Lubell, Huy Ong
Publikováno v:
Organic Letters. 23:3491-3495
Fifteen N-aminoimidazolone (Nai) dipeptides having a variety of 5-position side-chain groups were synthesized by regioselective proline-catalyzed reactions of azopeptide and aldehyde components followed by acid-mediated dehydration of an aza-aspartat
Autor:
Charity Deborah Yongo-Luwawa, Yousra Hamdane, Sitan Diarra, Mulamreddy Ramakotaiah, Pradeep S. Chauhan, Anh Minh Thao Nguyen, William D. Lubell, Xiaozheng Wei, Skye Brettell
Publikováno v:
Canadian Journal of Chemistry. 98:485-494
N′-Alkyl hydrazides were effectively synthesized by routes featuring installation, alkylation, and removal of a trifluoroacetyl group. A set of amino acid derived hydrazides were acylated using trifluoroacetic anhydride, and the resulting trifluoro
Publikováno v:
Canadian Journal of Chemistry. 98:278-284
N-Aminoimidazolone (Nai) peptide mimics were synthesized with minimal epimerization by base-promoted 5-endo-dig cyclization of aza-propargylglycine dipeptide acids and hydrazides followed by olefin migration. 5-Position functionalization using Mannic
Autor:
Yousra, Hamdane, Pradeep S, Chauhan, Suresh, Vutla, Mukandila, Mulumba, Huy, Ong, William D, Lubell
Publikováno v:
Organic letters. 23(9)
Fifteen