Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Edith J. Banner"'
Autor:
Edith J. Banner, Susan L. Mooberry, Jonathan E. Hempel, John T. Gupton, Milton L. Brown, Kimberly N. Weiderhold, Ernest Hamel, Anastasia Kharlamova, Sivanesan Dakshanamurthy
Publikováno v:
Molecular Pharmacology. 72:132-140
We studied the mechanism of action of 3,5-dibromo-4-(3,4-dimethoxyphenyl)-1H-pyrrole-2-carboxylic acid ethyl ester (JG-03-14) and found that it is a potent microtubule depolymerizer. JG-03-14 caused a dose-dependent loss of cellular microtubules, for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d26c0bafcd3c0d34a3c884f9c9dc137
https://doi.org/10.1124/mol.107.034876
https://doi.org/10.1124/mol.107.034876
Autor:
Anastasia Kharlamova, Jonathan E. Hempel, John T. Gupton, Keith Krumpe, Raymond N. Dominey, James A. Sikorski, Bradley K. Norwood, Barrett A. Little, Anthony Diebes, Shahnaz Ghassemi, Rene P.F. Kanters, Edith J. Banner, Charles R. Hickenboth, Matthew B. Coppock, Herman L. Holt, Bruce S. Burnham, Austin B. Scharf, Karen X. Du, Kartik M. Keertikar, Itta Bluhn-Chertudi, Melissa D. Sartin
Publikováno v:
Tetrahedron. 62:8243-8255
Studies directed on the synthesis of the pyrrole containing marine natural products Rigidin and Rigidin E via vinylogous iminium salts are described. The successful strategy relies on the formation of a 2,4-disubstituted pyrrole from a vinamidinium s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6e8e5631e95a30844cd36fe9b3a78ac
https://doi.org/10.1016/j.tet.2006.06.047
https://doi.org/10.1016/j.tet.2006.06.047
Autor:
Bret R. Adams, Robert B. Miller, Daniel W. Callahan, Nicholas E. Lauerman, Karen X. Du, Edith J. Banner, James A. Sikorski, John T. Gupton, Stuart C. Clough, Keith Krumpe, Kartik M. Keertikar, Barrett A. Little, John M. Solano, Austin B. Scharf, Rene P.F. Kanters
Publikováno v:
Tetrahedron. 61:1845-1854
A new and efficient relay synthesis of the marine natural products polycitone A and B is described. The new strategy relies on the formation of 2,4-disubstituted pyrroles from a vinamidinium salt followed by electrophilic substitution at the 5-positi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af83fd1cf6427017468f98a0f0417fa1
https://doi.org/10.1016/j.tet.2004.12.015
https://doi.org/10.1016/j.tet.2004.12.015
Publikováno v:
Tetrahedron Letters. 45:4411-4414
The Diels–Alder precursor was constructed from readily available d -glutamic acid utilizing a series of functional group transformations. The stereocenter of the amino acid provided the desired stereochemistry at C2 and diastereoselectively directe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39c3fea2f5a2703a72d1d69278863078
https://doi.org/10.1016/j.tetlet.2004.03.191
https://doi.org/10.1016/j.tetlet.2004.03.191
Autor:
Peter J. Barelli, Spencer R. Bates, Edith J. Banner, Nakul Telang, Kayleigh E. Hall, Rebecca Osterman, Kara L. Finzel, Xin Jia, Lauren T. Firich, R. Scott Welden, Matthew B. Coppock, John T. Gupton, John A. Stafford, Eric F. Worrall, Emily J. Kluball, James E. Eaton, Benjamin C. Giglio, Kerry Keertikar, Rene P.F. Kanters
Studies directed at the synthesis of (Z)-5-benzylidene-4-arylpyrrol-2(5H)-ones from (Z)-3-aryl-3-haloenoic acids are described. The successful strategy relies on the preparation of (Z)-3-aryl-3-haloenoic acids from acetophenones through the correspon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d528eea90de2115065c63b0408e9b66
https://europepmc.org/articles/PMC2997076/
https://europepmc.org/articles/PMC2997076/
Autor:
Ben C. Giglio, Matt J. Keough, Rene P.F. Kanters, Matthew B. Coppock, Melissa D. Sartin, Kristin L. Smith, James A. Sikorski, Timothy M. Smith, Edith J. Banner, Daniel C. Fisher, John T. Gupton, Jonathan E. Hempel, Anastasia Kharlamova, Raymond N. Dominey
Studies directed at the synthesis of polycitone and storniamide natural products via vinylogous iminium salts and microwave accelerated Vilsmeier-Haack formylations are described. The successful strategy relies on the formation of a 2,4-disubstituted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df1eeecc44472875e38da47aae3b1753
https://europepmc.org/articles/PMC2516947/
https://europepmc.org/articles/PMC2516947/