Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Thomas W. Scully"'
Autor:
Jo-Ann L. Stanton, Rory O'Brien, Richard J. Hall, Anastasia Chernyavtseva, Hye Jeong Ha, Lauren Jelley, Peter D. Mace, Alexander Klenov, Jackson M. Treece, John D. Fraser, Fiona Clow, Lewis Clarke, Yongdong Su, Harikrishnan M. Kurup, Vyacheslav V. Filichev, William Rolleston, Lee Law, Phillip M. Rendle, Lawrence D. Harris, James M. Wood, Thomas W. Scully, James E. Ussher, Jenny Grant, Timothy A. Hore, Tim V. Moser, Rhodri Harfoot, Blair Lawley, Miguel E. Quiñones-Mateu, Patrick Collins, Richard Blaikie
Publikováno v:
Frontiers in Public Health, Vol 9 (2022)
The rapid global rise of COVID-19 from late 2019 caught major manufacturers of RT-qPCR reagents by surprise and threw into sharp focus the heavy reliance of molecular diagnostic providers on a handful of reagent suppliers. In addition, lockdown and t
Externí odkaz:
https://doaj.org/article/c88caa11fedb42cf8990b491e7b3d6af
Autor:
Thomas W. Scully, Guy L. Plourde
Publikováno v:
Molecules, Vol 18, Iss 1, Pp 1174-1180 (2013)
A short five steps synthesis of the title compound from vanillin is described. The racemic spiroether 7 was obtained in 61% yield and in >99% diastereomeric excess (by 1H-NMR) from the corresponding phenolic derivative 3 by oxidation with lead (IV) a
Externí odkaz:
https://doaj.org/article/3f9fd25bb54244deabec0da9b5624a6b
Publikováno v:
Molecules, Vol 12, Iss 9, Pp 2215-2222 (2007)
The asymmetric syntheses of two new spirolactones prepared in optically pure form from L-3-nitrotyrosine are described. The key step, an oxidative spiroannulation, was carried out on the optically active phenols 11a and 11b and afforded the new spiro
Externí odkaz:
https://doaj.org/article/46438b12abc348fb85ca4a564ca111c2
Publikováno v:
Philosophical Transactions of the Royal Society B: Biological Sciences. 378
Anthranilate phosphoribosyltransferase catalyses the second reaction in the biosynthesis of tryptophan from chorismate in microorganisms and plants. The enzyme is homodimeric with the active site located in the hinge region between two domains. A ran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd960544947ad65eeb4708fd49460709
https://doi.org/10.1098/rstb.2022.0039
https://doi.org/10.1098/rstb.2022.0039
Publikováno v:
The Journal of Organic Chemistry. 81:12494-12498
The generation of dibrominated cyclopentenones via an interrupted Nazarov cyclization is reported. The installation of two bromine atoms occurs at the α and α' positions of the cyclopentenyl scaffold via successive nucleophilic and electrophilic br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fca8414b5a2daaca4402e7e138dcc5a2
https://doi.org/10.1021/acs.joc.6b02350
https://doi.org/10.1021/acs.joc.6b02350
Autor:
Frederick G. West, Olivier-Mohamad Soueidan, Victor Do, Frank Wuest, Jatinder Kaur, Alexandr Belovodskiy, Carson D. Matier, M. Joanne Lemieux, Thomas W. Scully, Rashmi Panigrahi, Chris I. Cheeseman
Publikováno v:
ACS chemical biology. 12(4)
The specificity characteristics of transporters can be exploited for the development of novel diagnostic therapeutic probes. The facilitated hexose transporter family (GLUTs) has a distinct set of preferences for monosaccharide substrates, and while
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a559aa7d1a64c2fc798cf70e232aab3
https://pubmed.ncbi.nlm.nih.gov/28205432
https://pubmed.ncbi.nlm.nih.gov/28205432
Autor:
Guy L. Plourde, Thomas W. Scully
Publikováno v:
Molecules
Volume 18
Issue 1
Pages 1174-1180
Molecules, Vol 18, Iss 1, Pp 1174-1180 (2013)
Volume 18
Issue 1
Pages 1174-1180
Molecules, Vol 18, Iss 1, Pp 1174-1180 (2013)
A short five steps synthesis of the title compound from vanillin is described. The racemic spiroether 7 was obtained in 61% yield and in >
99% diastereomeric excess (by 1H-NMR) from the corresponding phenolic derivative 3 by oxidation with lea
99% diastereomeric excess (by 1H-NMR) from the corresponding phenolic derivative 3 by oxidation with lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abec7f60ab0b3135a9832d7b340b09dc
https://doi.org/10.3390/molecules18011174
https://doi.org/10.3390/molecules18011174