Zobrazeno 1 - 10
of 18
pro vyhledávání: '"James T. Wasicak"'
Autor:
Badr Saeed, Douglas Kalvin, Patricia Ewing, Jerome Cohen, Saul H. Rosenberg, Henry Kenneth J, James T. Wasicak, Rolf E. Swenson, Sajeev Cherian, Michael J. Mitten, John J. Larsen, Andrew Tasker, Hing L. Sham, Shi-Chung Ng
Publikováno v:
Journal of Medicinal Chemistry. 42:4844-4852
Synthesis of a library of secondary benzylic amines based on the Sebti-Hamilton type peptidomimetic farnesyltransferase (FTase) inhibitor FTI-276 (1) led to the identification of 6 as a potent enzyme inhibitor (IC(50) of 8 nM) which lacked the proble
Autor:
Stephen P. Arneric, Michael Williams, David J.B. Kim, David J. Anderson, Yun He, Michael W. Decker, Diana L. Donnelly-Roberts, Theresa A. Kuntzweiler, Clark A. Briggs, Mark W. Holladay, Anthony W. Bannon, James T. Wasicak, Jeffrey E. Campbell, Keith B. Ryther, Nan-Horng Lin, Marietta Piattoni-Kaplan, Michael J. Buckley
Publikováno v:
Journal of Medicinal Chemistry. 41:407-412
New members of a previously reported series of 3-pyridyl ether compounds are disclosed as novel, potent analgesic agents acting through neuronal nicotinic acetylcholine receptors. Both (R)-2-chloro-5-(2-azetidinylmethoxy)pyridine (ABT-594, 5) and its
Autor:
James T. Wasicak, Richard Kasson, P Sullivan James, David J. Sweeny, Nan-Horng Lin, Yun He, J Anderson David
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:2389-2394
3′ and 5′-substituted pyrrolidine analogs of the potent cholinergic channel activator (ChCA), 3-methyl-5-(2(S)-pyrrolidinyl)-isoxazole (ABT 418), 1, were synthesized and tested in vitro for cholinergic channel receptor binding activity. Since the
Autor:
Michael J. Buckley, Stephen P. Arneric, James P. Sullivan, George M. Carrera, David S. Garvey, Michael W. Decker, Michael Williams, Jorge D. Brioni, Mark W. Holladay, James T. Wasicak
Publikováno v:
Journal of Medicinal Chemistry. 37:1055-1059
Autor:
James T. Wasicak, John Y. L. Chung
Publikováno v:
ChemInform. 22
Application of the Corey-Fuchs reaction on Boc-prolinal, Boc-4-hydroxyprolinal, Bocpiperidinal and Boc-serinal derivatives to give chiral 2-pyrrolidinyl-, 2-piperidinyl- and 4-oxazolidinyl-acetylene derivatives provided rapid access to a number of di
Autor:
James T. Wasicak, Michael Williams, D. S. Garvey, James P. Sullivan, Diana L. Donnelly-Roberts, Mark W. Holladay, Nan-Horng Lin, David E. Gunn, David J. Anderson, Yvonne C. Martin, P. A. Pavlik, Ann-Marie Hettinger, M. A. Abreo, Stephen P. Arneric
Publikováno v:
ChemInform. 27
Publikováno v:
Synthetic Communications. 22:1039-1048
The thermal lactamization of 4-(carboethoxy)-methyl-tryptophan ethyl ester (5), prepared from 4-(carboethoxy)methyl-indole 3 via Gilchrist′s method, in refluxing xylene followed by saponification provided the 8-membered cyclic tryptophan derivative
Autor:
James T. Wasicak, John Y. L. Chung
Publikováno v:
Tetrahedron Letters. 31:3957-3960
Application of the Corey-Fuchs reaction on Boc-prolinal, Boc-4-hydroxyprolinal, Bocpiperidinal and Boc-serinal derivatives to give chiral 2-pyrrolidinyl-, 2-piperidinyl- and 4-oxazolidinyl-acetylene derivatives provided rapid access to a number of di
Autor:
John Y. L. Chung, James T. Wasicak, Mark W. Holladay, William A. Arnold, Alex M. Nadzan, Catherine S. May
Publikováno v:
The Journal of Organic Chemistry. 55:270-275
La modification apportee dans la synthese de prolines substituees en 3 consiste en l'utilisation de triethyl silane et d'acide trifluoro acetique pour la reduction des pyrrolidine dicarboxylates-2,2 initiaux, et en la protection du N des prolines par
Autor:
Michael J. Dart, James T. Wasicak, Keith B. Ryther, Michael R. Schrimpf, Ki H. Kim, David J. Anderson, James P. Sullivan, Michael D. Meyer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f09f887cf1c865010a885462081ec39b
https://doi.org/10.1016/s0165-7208(00)80007-0
https://doi.org/10.1016/s0165-7208(00)80007-0