Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jeffery L. Harris"'
Autor:
Jeffery L. Harris, Moses Lee, William T. Pennington, Zarmeen T. Taherbhai, Lori Forrest, Martha Wicks, Michelle Stewart, Andrew M. Staples, Suzanna L. Bailey, Hari N. Pati
Publikováno v:
Letters in Drug Design & Discovery. 1:275-278
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::791824ed80dba739372a9ae1a09634cb
https://doi.org/10.2174/1570180043398821
https://doi.org/10.2174/1570180043398821
Autor:
John F. Payne, Joshua Hartwell, Timothy W. Hanks, Jeffery L. Harris, Dustin Phelps, April Crihfield, Rosa D. B. Walsh, William T. Pennington
Publikováno v:
Crystal Growth & Design. 3:313-320
The bis(aryl)diacetylenes 1,4-bis(3-quinolyl)-1,3-butadiyne (1), 1,4-bis(4-isoquinolyl)-1,3-butadiyne (2), and 1,4-bis(3-pyridyl)-1,3-butadiyne (3) form strongly halogen bonded complexes with organ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea581046187a78ba810f92d9e5ede637
https://doi.org/10.1021/cg0340042
https://doi.org/10.1021/cg0340042
Autor:
Toni Brown, Herman L. Holt, Moses Lee, Hari N. Pati, Hadi D. Arman, Jeffery L. Harris, John Dickson, Don VanDerveer, Regan M. LeBlanc, William T. Pennington, Michelle Stewart
Publikováno v:
Bioorganicmedicinal chemistry. 13(21)
Twenty-six epoxide and corresponding pyrazole derivatives, of the structurally related chalcones and combretastatin A-4 (CA-4), were synthesized and tested for in vitro cytotoxicity. These molecules were synthesized by epoxidation of the relevant cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1459b22d7a7bc3934499652a1626f0e1
https://pubmed.ncbi.nlm.nih.gov/16055334
https://pubmed.ncbi.nlm.nih.gov/16055334
Autor:
William T. Pennington, Stephen E. Creager, Jeffery L. Harris, Darryl D. DesMarteau, Jennie R. Atkins, C. R. Sides, S. C. Savett, Brian Thomas
Publikováno v:
Journal of The Electrochemical Society. 149:A1527
Two structurally related perfluorinated ionomer materials, one a conventional sulfonic-acid-batred ionomer (Nafion) and the other an experimental bis[(perfluoroalkyl)sulfonyl]imide-based ionomer in which the sulfonic acid group has been replaced by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd1897d7eb5c4609498a1a9e43e148d5
https://doi.org/10.1149/1.1516218
https://doi.org/10.1149/1.1516218