Zobrazeno 1 - 10
of 96
pro vyhledávání: '"G. VON SPRECHER"'
Autor:
W. FROESTL, S. J. MICKEL, G. VON SPRECHER, P. J. DIEL, R. G. HALL, L. MAIER, D. STRUB, V. MELILLO, P. A. BAUMANN, R. BERNASCONI, C. GENTSCH, K. HAUSER, J. JAEKEL, G. KARLSSON, K. KLEBS, L. MAITRE, C. MARESCAUX, M. F. POZZA, M. SCHMUTZ, M. W. STEINMANN, H. VAN RIEZEN, A. VASSOUT, et al. et al.
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3995c65cd3af15e70de0e6c0775aa257
https://doi.org/10.1002/chin.199551215
https://doi.org/10.1002/chin.199551215
Autor:
Stuart J. Mickel, Grety Rihs, Roger Graham Hall, P. C. Waldmeier, Conrad Gentsch, G. Von Sprecher, J. Jaekel, Helmut Bittiger, P. A. Baumann, Wolfgang Froestl, H. R. Olpe, Dietrich Strub, Felix Brugger, Annick Vassout
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::204bdc116be98cddced44ef913593f8e
https://doi.org/10.1002/chin.199551214
https://doi.org/10.1002/chin.199551214
Autor:
P. C. Waldmeier, J. J. Feldtrauer, P. A. Baumann, Serge Bischoff, Helmut Bittiger, G. Von Sprecher, Kathleen Hauser
Publikováno v:
Naunyn-Schmiedeberg's Archives of Pharmacology. 342:305-311
CGP 28014 (N-(2-pyridone-6-yl)-N',N'-di-n-propylformamidine) or its methanesulfonate salt CGP 28014 A was suspected to be a catechol-O-methyl-transferase (COMT) inhibitor because it was found to reduce the levels of homovanillic acid (HVA) and to inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6701c3fa1879451bd79706c3f871761
https://doi.org/10.1007/bf00169442
https://doi.org/10.1007/bf00169442
Autor:
W, Froestl, S J, Mickel, R G, Hall, G, von Sprecher, D, Strub, P A, Baumann, F, Brugger, C, Gentsch, J, Jaekel, H R, Olpe
Publikováno v:
Journal of medicinal chemistry. 38(17)
The antispastic agent and muscle relaxant baclofen 1 is a potent and selective agonist for bicuculline-insensitive GABAB receptors. For many years efforts to obtain superior GABAB agonists were unsuccessful. We describe the syntheses and biological p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab88d29f1dcebe8d9429354d5e7fa96a
https://pubmed.ncbi.nlm.nih.gov/7650684
https://pubmed.ncbi.nlm.nih.gov/7650684
Publikováno v:
Drugs of the Future. 17:275
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54ce8c11e25b808cd7db578d36bac3a2
https://doi.org/10.1358/dof.1992.017.04.170294
https://doi.org/10.1358/dof.1992.017.04.170294
Publikováno v:
Tetrahedron Letters. 20:1905-1908
The variable exo/endo rate ratios observed in the solvolysis of 6-exo-substituted exo- and endo-2-norbornyl p-toluenesulfonates are due to differential transmission of polar effects in the transition state for ionization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1d88558af1624a037b4ef70c3708a16
https://doi.org/10.1016/s0040-4039(01)86875-1
https://doi.org/10.1016/s0040-4039(01)86875-1
Publikováno v:
Tetrahedron Letters. 20:473-476
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5e96c91d937849284df71fd1d3301be
https://doi.org/10.1016/s0040-4039(01)93536-1
https://doi.org/10.1016/s0040-4039(01)93536-1
Publikováno v:
Tetrahedron Letters. 20:1901-1904
The solvolysis rates of endo-2-norbornyl p-toluenesulfonates 1 are affected far less by 6-exo-substituents than are the rates of the corresponding exo-2-norbornyl p-toluenesulfonates 2 1.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::128fbcb71bcab28ea2321c540b600424
https://doi.org/10.1016/s0040-4039(01)86874-x
https://doi.org/10.1016/s0040-4039(01)86874-x
Publikováno v:
Chemischer Informationsdienst. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db4ce5619fc1cb0d223de5dfe4127dc0
https://doi.org/10.1002/chin.198411088
https://doi.org/10.1002/chin.198411088
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43ac4c9845508e63defe4d8f716103bf
https://doi.org/10.1002/chin.198212117
https://doi.org/10.1002/chin.198212117