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pro vyhledávání: '"Claire Herby"'
Publikováno v:
Organic Letters. 17:5626-5629
To increase the chemical diversity accessible with peptoids and peptide-peptoid hybrids, N-alkylated arylsulfonamides were used to prepare side chain protected N-substituted glycines compatible with solid-phase synthesis. The described procedures giv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2eebd28eae5fba68536b7bba09aae3d
https://doi.org/10.1021/acs.orglett.5b02862
https://doi.org/10.1021/acs.orglett.5b02862
Publikováno v:
Peptides 2015, Proceedings of the 24th American Peptide Symposium.
Peptoids (oligo N-substituted glycines) are peptidomimetic oligomers showing attractive structural and pharmacological properties for the development of therapeutic candidates and molecular tools [1,2]. Compared to peptides, peptoids are resistant to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c6c7499cd46a81729a315f4fba7b907
https://doi.org/10.17952/24aps.2015.280
https://doi.org/10.17952/24aps.2015.280
Publikováno v:
Organic Letters; Nov2015, Vol. 17 Issue 22, p5626-5629, 4p