Zobrazeno 1 - 10
of 14
pro vyhledávání: '"T. S. Yokum"'
Publikováno v:
Journal of Peptide Research. 59:9-17
A collection of natural peptides, simplified analogs of natural peptides, de novo amphipathic peptides and de novo amphipathic peptides composed of 50-80% alpha,alpha-dialkylated glycines (alpha,alpha-Dags) were synthesized on solid-phase resin as th
Autor:
Rebekah L. Gundry, Mark L. McLaughlin, T. S. Yokum, C. L. Wysong, Guillermo A. Morales, Robert P. Hammer
Publikováno v:
ChemInform. 28
Publikováno v:
ChemInform. 28
Publikováno v:
ChemInform. 28
Publikováno v:
ChemInform. 28
α,α-Disubstituted amino acids can be used to choose the desired helical structure of a peptide. This ability could lead to stble antimicrobial agents
Autor:
Frank R. Fronczek, T. S. Yokum, Y.-H. Liu, Ted J. Gauthier, Mark L. McLaughlin, Guillermo A. Morales
Publikováno v:
ChemInform. 29
Cyclohexanespiro-5'-hydantoin monohydrate, C8H12N2O2.H2O, has a chair-shaped cyclohexane ring with endocyclic torsion-angle magnitudes in the range 54.4 (2)-56.3 (2) degrees. All potential hydrogen-bond donors are involved in intermolecular hydrogen
Publikováno v:
American Peptide Symposia ISBN: 0792351606
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b714fd402c8fe952c8571569d4a0ad17
https://doi.org/10.1007/0-306-46862-x_141
https://doi.org/10.1007/0-306-46862-x_141
Publikováno v:
American Peptide Symposia ISBN: 0792351606
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f58df01e42a304538c39abbe0b4867b4
https://doi.org/10.1007/0-306-46862-x_142
https://doi.org/10.1007/0-306-46862-x_142
Publikováno v:
American Peptide Symposia ISBN: 0792351606
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a095d54f46f1c81475fc837382ba650
https://doi.org/10.1007/0-306-46862-x_286
https://doi.org/10.1007/0-306-46862-x_286
Publikováno v:
The Journal of organic chemistry. 64(24)
A novel and general backbone amide linker (BAL) strategy has been devised for preparation of C-terminal modified peptides containing hindered, unreactive, and/or sensitive moieties, in concert with N(alpha)()-9-fluorenylmethoxycarbonyl (Fmoc) solid-p