Zobrazeno 1 - 10
of 398
pro vyhledávání: '"J. Guiry"'
Autor:
Lucy Byrne, Patrick J. Guiry
Publikováno v:
Molecules, Vol 29, Iss 10, p 2233 (2024)
This review article assembles key recent advances in the synthetic chemistry and biology of specialised pro-resolving mediators (SPMs). The major medicinal chemistry developments in the design, synthesis and biological evaluation of synthetic SPM ana
Externí odkaz:
https://doaj.org/article/c2a13370d72c450c93c8b37ccbe755a4
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-9 (2022)
Isotopic analyses of bone collagen from 95 archaeological short-tailed albatross specimens explore long-term patterns in foraging characteristics and individual foraging site fidelity of birds off of Vancouver Island.
Externí odkaz:
https://doaj.org/article/f132c7b6dca24965a0351ad1af19cceb
Publikováno v:
Frontiers in Ecology and Evolution, Vol 10 (2022)
Sulfur isotope (δ34S) analyses are an important archaeological and ecological tool for understanding human and animal migration and diet, but δ34S can be difficult to interpret, particularly in archaeological human-mobility studies, when measured i
Externí odkaz:
https://doaj.org/article/fcb912a02d8b4db897bfead54d743f1c
Autor:
Thomas C. A. Royle, Eric. J. Guiry, Hua Zhang, Lauren T. Clark, Shalegh M. Missal, Sophie A. Rabinow, Margaretta James, Dongya Y. Yang
Publikováno v:
Ecology and Evolution, Vol 12, Iss 8, Pp n/a-n/a (2022)
Abstract The short‐tailed albatross (Phoebastria albatrus) is a threatened seabird whose present‐day range encompasses much of the North Pacific. Within this species, there are two genetic clades (Clades 1 and 2) that have distinctive morphologie
Externí odkaz:
https://doaj.org/article/230fae219cd14d69ac8424396c602ae3
Publikováno v:
Molecules, Vol 27, Iss 18, p 6078 (2022)
Herein, we report the design and synthesis of a series of chiral pyrrolidine-substituted ferrocene-derived ligands. The proficiency of this novel structural motif was demonstrated in the Rh-catalyzed asymmetric hydrogenation of dehydroamino acid este
Externí odkaz:
https://doaj.org/article/8842fbf75a3847799203ecb4944bd846
Publikováno v:
Transition‐Metal‐Catalyzed C‐H Functionalization of Heterocycles. :435-484
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::405640d03d8e80b65f290365f92fcd7f
https://doi.org/10.1002/9781119774167.ch10
https://doi.org/10.1002/9781119774167.ch10
Publikováno v:
Synthesis. 55:1274-1284
Lipoxins are an important class of pro-resolving mediators that play a crucial role in the resolution of inflammation. Thus, the synthesis of more metabolically stable synthetic lipoxin analogues is an area of significant interest. Herein the asymmet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56b3566610331e610c39855fc24afbc4
https://doi.org/10.1055/a-1992-7148
https://doi.org/10.1055/a-1992-7148
Publikováno v:
Synlett. 33:1841-1846
The synthesis of a series of planar chiral P,N-ferrocenylpyrrolidine-containing ligands, with varying substituents at the phosphorus donor atom, is described. The phosphorus donor atom was introduced via a diastereoselective ortho-directed metalation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f95e83ef3d698c9d2a67c75e0d92408
https://doi.org/10.1055/s-0042-1752342
https://doi.org/10.1055/s-0042-1752342
Autor:
Joseph Breheny, Cian Kingston, Robert Doran, Joao Anes, Marta Martins, Séamus Fanning, Patrick J. Guiry
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 12, p 6400 (2021)
Herein, we report antibacterial and antifungal evaluation of a series of previously prepared (+)-tanikolide analogues. One analogue, (4S,6S)-4-methyltanikolide, displayed promising anti-methicillin-resistant Staphylococcus aureus activity with a MIC
Externí odkaz:
https://doaj.org/article/c335569cede9428a826dd922091585b4
Publikováno v:
Organic Letters. 24:6049-6053
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e238061a44676ce77d44b0f797e9823e
https://doi.org/10.1021/acs.orglett.2c02345
https://doi.org/10.1021/acs.orglett.2c02345