Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Julian M. Davis"'
Autor:
Donald Sikazwe, Bereket Mochona, Kwan Hon Cheng, William Horton, Rukhsar Banu, Julian M. Davis, Cynthia Franklin, Jason S. Gerding, Muziya Nakazwe, Marianna Török
Publikováno v:
Scientia Pharmaceutica
Scientia Pharmaceutica, Vol 86, Iss 1, p 2 (2017)
Scientia Pharmaceutica, Vol 86, Iss 1, p 2 (2017)
The objective of this research is to generate leads for developing our ultimate poly-active molecules with utility in central nervous system (CNS) diseases. Indeed, poly-active molecules capable of mitigating brain free radical damage while enhancing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e9e830c5bb74c763286abcbd837301a
https://pubmed.ncbi.nlm.nih.gov/29267246
https://pubmed.ncbi.nlm.nih.gov/29267246
Autor:
Jonathan L. Sessler, D. Webster Keogh, Vladimír Král, Julian M. Davis, Norman L. Schroeder, Anne E. V. Gorden
Publikováno v:
Supramolecular Chemistry. 16:91-100
The addition of aqueous pH 7 solutions of 7.2×10-3 M pertechnetate to dilute aqueous 2.5% MeOH solutions containing a water-solubilized sapphyrin, 3,12,13,22-tetraethyl-8,17-bis[bis(hydroxyethyl)-amino)carbonylethyl]-2,7,18,23-tetramethylsapphyrin (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dedd589c947125aad9c017fafdc975a
https://doi.org/10.1080/10610270310001626464
https://doi.org/10.1080/10610270310001626464
Publikováno v:
Tetrahedron Letters. 42:2447-2450
Sapphyrins may be obtained in ca. 30% yield via the condensation of 1 equivalent of a tripyrrane dialdehyde with 2 equivalents of a β-substituted pyrrole, followed by oxidation with DDQ.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9eaa1b8ffcfea2e5a0ce2cf1d2de1fc6
https://doi.org/10.1016/s0040-4039(01)00198-8
https://doi.org/10.1016/s0040-4039(01)00198-8
Publikováno v:
Journal of Chemical Education. 88:232-234
A high-performance liquid chromatography experiment to determine the concentration of caffeine and vitamin B6 in sports energy drinks has been developed. This laboratory activity, which is appropriate for an upper-level instrumental analysis course,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64270773dab3fabc02e8b9edcaba7670
https://doi.org/10.1021/ed100146s
https://doi.org/10.1021/ed100146s
Autor:
Greg Hemmi, Vincent M. Lynch, Pavel Anzenbacher, Tarak D. Mody, Bruno Andrioletti, Wataru Sato, Andrew C. Try, Darren Magda, Karolina Jursíková, Nicolai A. Tvermoes, Christopher B. Black, Julian M. Davis, Daniel Seidel, Jonathan L. Sessler, Vladimír Král
Publikováno v:
Scopus-Elsevier
A number of aromatic and nonaromatic expanded porphyrins have been prepared in the authors' laboratories. These are allowing a number of important themes to be explored, including the construction of novel cation- and anion-complexing agents and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5649ebab5efbe1056a6e3c3ff905386
https://doi.org/10.1351/pac199971112009
https://doi.org/10.1351/pac199971112009
Publikováno v:
ChemInform. 32
Sapphyrins may be obtained in ca. 30% yield via the condensation of 1 equivalent of a tripyrrane dialdehyde with 2 equivalents of a β-substituted pyrrole, followed by oxidation with DDQ.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a06fa7e5660bf5cef6d42a47214d93b8
https://doi.org/10.1002/chin.200126104
https://doi.org/10.1002/chin.200126104
Autor:
Julian M. Davis, Jonathan L. Sessler
Publikováno v:
ChemInform. 33
Sapphyrin was the first expanded porphyrin to be reported in the literature and remains among the most extensively studied. Much of the interest in this macrocycle reflects its ability to bind anions, a phenomenon that has been examined in solution a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4593294b67cd750c6ee2d1c3c83796bf
https://doi.org/10.1002/chin.200213260
https://doi.org/10.1002/chin.200213260
Publikováno v:
Organicbiomolecular chemistry. 1(22)
As part of an ongoing effort to study the anion binding properties of sapphyrins in various media, a number of previously reported water solubilized sapphyrins were studied in methanol and in buffered, neutral aqueous solutions and found to undergo s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7043d0a8e89875fffb31617ce5fec525
https://pubmed.ncbi.nlm.nih.gov/14664401
https://pubmed.ncbi.nlm.nih.gov/14664401
Autor:
Julian M. Davis, Jonathan L. Sessler
Publikováno v:
Accounts of chemical research. 34(12)
Sapphyrin was the first expanded porphyrin to be reported in the literature and remains among the most extensively studied. Much of the interest in this macrocycle reflects its ability to bind anions, a phenomenon that has been examined in solution a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f5a74382de34234088ed7421bae6fc7
https://pubmed.ncbi.nlm.nih.gov/11747417
https://pubmed.ncbi.nlm.nih.gov/11747417
Publikováno v:
The Journal of organic chemistry. 63(20)
The synthesis of 16,20-dipropyl-2,3,6,7,10,11,15,21-octamethyl-[22]pentaphyrin-(1.1.1.0.0) (8), a stable isomer of smaragdyrin ([22]pentaphyrin(1.1.0.1.0)), and 9, a furan-containing analogue of 8, are reported. These two new expanded porphyrins were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f89d1d8ac3405f150fc466c4d6b57c23
https://pubmed.ncbi.nlm.nih.gov/11672332
https://pubmed.ncbi.nlm.nih.gov/11672332