Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Katarina J, Makaravage"'
Autor:
Andrew V. Mossine, Allen F. Brooks, Naoko Ichiishi, Katarina J. Makaravage, Melanie S. Sanford, Peter J. H. Scott
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Abstract In a relatively short period of time, transition metal-mediated radiofluorination reactions have changed the PET radiochemistry landscape. These reactions have enabled the radiofluorination of a wide range of substrates, facilitating access
Externí odkaz:
https://doaj.org/article/7daafde7551a4666b9c628beed7fc804
Publikováno v:
Nuclear Medicine and Biology. :56-86
Hydrogen cyanide (HCN) is a versatile synthon for generating carbon‑carbon and carbon-heteroatom bonds. Unlike other one-carbon synthons (i.e., CO, CO2), HCN can function as a nucleophile (as in potassium cyanide, KCN) and an electrophile (as in cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccd44a3951f28b1d048fb734654b4cf0
https://doi.org/10.1016/j.nucmedbio.2021.09.002
https://doi.org/10.1016/j.nucmedbio.2021.09.002
Autor:
So Jeong Lee, Katarina J. Makaravage, María T Morales-Colón, Jay S. Wright, Peter J. H. Scott, Melanie S. Sanford, Allen F. Brooks
Publikováno v:
J Org Chem
This report describes a method for the nucleophilic radiofluorination of (hetero)aryl chlorides, (hetero)aryl triflates, and nitroarenes using a combination of [(18)F]KF•K(2.2.2) and Me(4)N HCO(3) for the in situ formation of a strongly nucleophili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf2781ca0e3fc07a7c34398a945feae4
https://doi.org/10.1021/acs.joc.1c01491
https://doi.org/10.1021/acs.joc.1c01491
Autor:
Sameer Tyagi, Bruce P. McKillican, Tolani K. Salvador, Moses G. Gichinga, William J. Eberle, Russell Viner, Katarina J. Makaravage, Trey S. Johnson, C. Adam Russell, Subho Roy
Publikováno v:
The Journal of organic chemistry. 87(9)
A bioinspired synthesis of Pinoxaden metabolites
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6dcc9eb9f230653c10a36e60505d987
https://pubmed.ncbi.nlm.nih.gov/35442682
https://pubmed.ncbi.nlm.nih.gov/35442682
Autor:
Melanie S. Sanford, Allen F. Brooks, Katarina J. Makaravage, Peter J. H. Scott, Jay S. Wright
Publikováno v:
Handbook of Radiopharmaceuticals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::375c31935ab25ecf2ef4fec170b2f1cd
https://doi.org/10.1002/9781119500575.ch8
https://doi.org/10.1002/9781119500575.ch8
Autor:
Skylar Norman, Katarina J. Makaravage, Amanda C. Jones, Yuyang Zhu, Brock R. Yager, Ruichen Lan, Dwaine D. Hodges, Cynthia S. Day, Wentong Zhou, Fred L. Liu, Carolin Griebel
Publikováno v:
Organometallics. 39:2665-2671
This paper describes the synthesis and characterization of RP(o-biphenyl)2 phosphine ligands (where R = PhO, Ph, and t-Bu), corresponding gold(I) chloride precatalysts, gold(I) triflate catalysts, and gold(I) π-complexes. All ligands and gol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2f4ef3beb0cdfb7258af8cd84b17e98
https://doi.org/10.1021/acs.organomet.0c00278
https://doi.org/10.1021/acs.organomet.0c00278
Autor:
Thomas Erhard, Melanie S. Sanford, Christian Bruetting, Sean S. Tanzey, Bradford D. Henderson, Andrew V. Mossine, Jason Miller, Naoko Ichiishi, Peter J. H. Scott, Allen F. Brooks, Marc B. Skaddan, Katarina J. Makaravage
Publikováno v:
Nature Protocols. 15:1742-1759
[18F]6-fluoro-L-DOPA ([18F]FDOPA) is a diagnostic radiopharmaceutical for positron emission tomography (PET) imaging that is used to image Parkinson's disease, brain tumors, and focal hyperinsulinism of infancy. Despite these important applications,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8477b4be1bab09643f33bccd3ceafb12
https://doi.org/10.1038/s41596-020-0305-9
https://doi.org/10.1038/s41596-020-0305-9
Autor:
Katarina J. Makaravage, Peter J. H. Scott, Wade Winton, Allen F. Brooks, Liam S. Sharninghausen, Melanie S. Sanford
Publikováno v:
J Am Chem Soc
[(18)F]-labeled aryl fluorides are widely used as radiotracers for positron emission tomography (PET) imaging. Aryl halides (ArX) are particularly attractive precursors to these radiotracers, as they are readily available, inexpensive, and stable. Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b1f8f795b466a2c1815c6d0fe88ee91
https://doi.org/10.1021/jacs.0c02637
https://doi.org/10.1021/jacs.0c02637
Publikováno v:
Angewandte Chemie International Edition. 58:3119-3122
A Cu-mediated ortho-C-H radiofluorination of aromatic carboxylic acids that are protected as 8-aminoquinoline benzamides is described. The method uses K18 F and is compatible with a wide range of functional groups. The reaction is showcased in the hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cb9d19ea9f2a8af07745ce87d78ce26
https://doi.org/10.1002/anie.201812701
https://doi.org/10.1002/anie.201812701
Autor:
Allen F. Brooks, So Jeong Lee, Katarina J. Makaravage, Peter J. H. Scott, Melanie S. Sanford, Andrew V. Mossine, Naoko Ichiishi
Publikováno v:
Chemical Communications. 55:2976-2979
This report describes a Pd-mediated C–H radiofluorination of 8-methylquinoline derivatives with no-carrier-added Ag[18F]F. To achieve this transformation, a new method was developed for the generation of Ag[18F]F using a sep-pak cartridge. The C–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d746d4ca3bcc425561eaba65c5e4f071
https://doi.org/10.1039/c9cc00641a
https://doi.org/10.1039/c9cc00641a