Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Jennifer L. Stockdill"'
Publikováno v:
ACS Central Science, Vol 9, Iss 4, Pp 590-592 (2023)
Externí odkaz:
https://doaj.org/article/452f541a9c7b42c9a0c1e66d47df809a
Autor:
Arthur Zastepa, Judy A. Westrick, Anqi Liang, Johnna A. Birbeck, Elliot Furr, L. Cynthia Watson, Jennifer L. Stockdill, Boddu S. Ramakrishna, Sophie Crevecoeur
Publikováno v:
Journal of Great Lakes Research. 49:134-146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf31164fb1e9a39bf7a88473be5eb6b4
https://doi.org/10.1016/j.jglr.2022.12.006
https://doi.org/10.1016/j.jglr.2022.12.006
Autor:
Naresh M. Venneti, Ganesh Samala, Rana M. I. Morsy, Lawrence G. Mendoza, Albert Isidro-Llobet, Janine K. Tom, Subha Mukherjee, Michael E. Kopach, Jennifer L. Stockdill
Publikováno v:
Journal of the American Chemical Society. 145:1053-1061
Peptides are steadily gaining importance as pharmaceutical targets, and efficient, green methods for their preparation are critically needed. A key deficiency in the synthetic toolbox is the lack of an industrially viable peptide desulfurization meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::763026e5b2c369a214dab07b540fdce8
https://doi.org/10.1021/jacs.2c10625
https://doi.org/10.1021/jacs.2c10625
Publikováno v:
Org Biomol Chem
C-Terminally modified peptides are important for the development and delivery of peptide-based pharmaceuticals because they impact peptide activity, stability, hydrophobicity, and membrane permeability. Additionally, the vulnerability of C-terminal e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13fdaf4ebf9318dfb95c467dd6444c42
https://doi.org/10.1039/d0ob01417f
https://doi.org/10.1039/d0ob01417f
Publikováno v:
Chemical Science. 10:10475-10480
Studies of S-linked glycoconjugates have attracted growing interest because of their enhanced chemical stability and enzymatic resistance over O-glycoside counterparts. We here report a facile approach to access α-1,2-cis-S-linked glycosides using t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87501acc3303cd002265444abf9912b3
https://doi.org/10.1039/c9sc04079j
https://doi.org/10.1039/c9sc04079j
Publikováno v:
Tetrahedron Letters. 59:3903-3906
In this manuscript, we establish the susceptibility of the N-methyldiaminobenzoyl linker to undergo undesired acylation during standard peptide capping with acetic anhydride. Successive capping treatments led to problematic levels of linker incapacit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea769f2fd67d9629deab1182d7a433cf
https://doi.org/10.1016/j.tetlet.2018.08.061
https://doi.org/10.1016/j.tetlet.2018.08.061
Autor:
Hansamali S. Sirinimal, H. Bernhard Schlegel, Gregory J. Rosenhauer, Heng Chen, Ganesh Samala, Sebastien P. Hebert, Jennifer L. Stockdill
Publikováno v:
Organic Letters. 20:6340-6344
5- exo, 5- exo Cyclizations of conformationally unbiased propargylic aminyl radicals proceed with excellent yield, chemoselectivity, and diastereoselectivity under tin-free reductive cyclization conditions, regardless of the electronic environments a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f301db662a702bceb9d952a2994ffc0b
https://doi.org/10.1021/acs.orglett.8b02456
https://doi.org/10.1021/acs.orglett.8b02456
Autor:
Alberto M. Lopez, Ahmad A. Ibrahim, Gregory J. Rosenhauer, Hansamali S. Sirinimal, Jennifer L. Stockdill
Publikováno v:
Organic Letters. 20:2216-2219
A tin-free strategy for the successful cyclization of a variety of internal alkyne-containing N-chloroamine precursors to the ABC core via cyclization of a neutral aminyl radical is established. Deuterium labeling experiments confirm that the solvent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1235cfeb654ca2d4c0f3fc16c8c0aa2
https://doi.org/10.1021/acs.orglett.8b00544
https://doi.org/10.1021/acs.orglett.8b00544
Autor:
John A. Brailsford, Jennifer L. Stockdill, Eric V. Johnston, Abram J. Axelrod, Paul A. Vadola, Samuel J. Danishefsky, Michael T. Peterson
Publikováno v:
Tetrahedron. 74:1951-1956
The β-subunit of human thyroid stimulating hormone (hTSH) has been synthesized as a single glycoform bearing a chitobiose disaccharide at the native glycosylation site. Key to the successful completion of this synthesis was the introduction of an ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c8922168370d39e468501e1414bb3bb
https://doi.org/10.1016/j.tet.2018.02.067
https://doi.org/10.1016/j.tet.2018.02.067
Publikováno v:
The Journal of Organic Chemistry. 83:1797-1803
Sequence diversification at the C terminus is traditionally limited by significant epimerization of the C-terminal residue during its activation toward nucleophilic attack, thus mandating repetition of the peptide synthesis for each targeted variatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec04ba7238a0799389438cce6b67f755
https://doi.org/10.1021/acs.joc.7b02655
https://doi.org/10.1021/acs.joc.7b02655