Zobrazeno 1 - 10
of 11
pro vyhledávání: '"T. J. REITZ"'
Autor:
Vidyadhar M. Paradkar, T. J. Reitz, Daniel J. Sall, Moorthy S. S. Palanki, Aldean J. Kolar, Gary L. Grunewald
Publikováno v:
ChemInform. 22
(1990). ONE-STEP SYNTHESIS OF TRIFLUOROMETHYL- AND OF METHOXY-SUBSTITUTED BENZYNE PRECURSORS. Organic Preparations and Procedures International: Vol. 22, No. 6, pp. 747-753.
Autor:
Moorthy S. S. Palanki, Daniel J. Sall, Vidyadhar M. Paradkar, T. J. Reitz, Aldean J. Kolar, Gary L. Grunewald
Publikováno v:
Organic Preparations and Procedures International. 22:747-753
(1990). ONE-STEP SYNTHESIS OF TRIFLUOROMETHYL- AND OF METHOXY-SUBSTITUTED BENZYNE PRECURSORS. Organic Preparations and Procedures International: Vol. 22, No. 6, pp. 747-753.
Autor:
A. Hallett, J M Archuleta rd, Gary L. Grunewald, James A. Ruth, S. Vollmer, T. J. Reitz, C. O. Rutledge
Publikováno v:
Journal of Medicinal Chemistry. 23:614-620
Autor:
Charles O. Rutledge, Gary L. Grunewald, James A. Ruth, Sheila Vollmer, Lee E. Elden, T. J. Reitz
Publikováno v:
Biochemical Pharmacology. 28:417-421
In order to assess the importance of the aromatic rings in inhibition of neuronal amine uptake produced by tricyclic antidepressant drugs, derivatives of imipramine (IMI) and dcsipramine (DMI) were prepared in which either one (IMIH, DMIH) or both (I
Autor:
Gary L. Grunewald, T. J. Reitz
Publikováno v:
Organic Magnetic Resonance. 21:596-601
13C nuclear magnetic resonance spectra were collected for a series of 5- and 6-monoaromatic ring-substituted benzonorbornadienes and 5-, 6-, 7-, and 8-monosubstituted benzonorbornen-2-ones. 13C chemical shifts values were found to be useful in the di
Autor:
C. O. Rutledge, James A. Ruth, A. Hallett, Gary L. Grunewald, T. J. Reitz, S. Vollmer, J. M. Iii Archuleta
Publikováno v:
Chemischer Informationsdienst. 11
Autor:
Gary L. Grunewald, Bharak Pazhenchevsky, Daniel J. Sall, Michael A. Pleiss, T. J. Reitz, Vidyadhar M. Paradkar, William L. Seibel
Publikováno v:
Chemischer Informationsdienst. 14
Publikováno v:
ChemInform. 18
In order to determine the active site binding orientation of norepinephrine, a series of conformationally defined analogues of the tyramines, in which the ethylamine side chain is held fixed by incorporation into a benzonorbornene skeleton, were prep
Autor:
D. G. FARNUM, T. VEYSOGLU, A. M. CARDE, R. T. CARDE, B. DUHL-EMSWILER, T. A. PANCOAST, T. J. REITZ
Publikováno v:
Chemischer Informationsdienst. 9
Publikováno v:
Journal of medicinal chemistry. 29(10)
In order to determine the active site binding orientation of norepinephrine, a series of conformationally defined analogues of the tyramines, in which the ethylamine side chain is held fixed by incorporation into a benzonorbornene skeleton, were prep