Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Dieter Binder"'
Publikováno v:
Tetrahedron. 56:3697-3701
A rapid route was developed to afford ethynyl-substituted imidazole derivatives which served as key compounds for aryl–alkynyl-coupling reactions. Addition of mono-silylated acetylene to O-protected oximes was carried out in the absence of Lewis ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e14fc8b521efebba0477ab25aa2afc53
https://doi.org/10.1016/s0040-4020(00)00306-9
https://doi.org/10.1016/s0040-4020(00)00306-9
Publikováno v:
Monatshefte für Chemie / Chemical Monthly. 130:645-651
The synthesis of the thiophene analogue of dazoxiben – one of the most selective TXA 2-synthase inhibitors – and its derivatization to a chlorinated, more lipophilic product is described. The ethylenoxy moiety was introduced via nucleophilic arom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8490981560e5c64fcaa9b1ccc3d5a4c9
https://doi.org/10.1007/pl00010245
https://doi.org/10.1007/pl00010245
Publikováno v:
Monatshefte für Chemie / Chemical Monthly. 129:887-896
The synthesis of three thiophene analogues of Flosulide – a potent and selective inhibitor of cyclooxygenase subtype 2 (COX-2) – is described. Utilizing combined Friedel-Crafts acylation and alkylation of 2-chlorothiophene, simplified procedures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25cce3a2b1f49a0689755c8eb5ec12fe
https://doi.org/10.1007/pl00013496
https://doi.org/10.1007/pl00013496
Publikováno v:
Journal of Heterocyclic Chemistry. 35:923-926
Three isomeric substituted thienoimidazothiazoles were synthesized as thiophene analogs of the immune modulator TILOMISOL, by cyclizing appropriate β-oxothioethers of thienoimidazoles. In contrast to the benzene analog no intermediates were observed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a3682639cfbc93e60f79dfce92d8100
https://doi.org/10.1002/jhet.5570350423
https://doi.org/10.1002/jhet.5570350423
Publikováno v:
Synthesis. 1978:60-62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ac925f90ed7adcd05b4e3518e4bfb6a
https://doi.org/10.1055/s-1978-25386
https://doi.org/10.1055/s-1978-25386
Publikováno v:
Tetrahedron Letters. 43:177-179
Both enantiomers of the conformationally restricted nicotine analogue 7-(3-pyridyl)-1-azabicyclo[2.2.1]heptane were prepared in a convenient, asymmetric synthetic route.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2be53be5f5b262fe047e6139d92cd986
https://doi.org/10.1016/s0040-4039(01)01985-2
https://doi.org/10.1016/s0040-4039(01)01985-2
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa900a34107841b260eb401677508340
https://doi.org/10.1002/chin.199125157
https://doi.org/10.1002/chin.199125157
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ee629007f9f77a5ac4c97739159d4ac
https://doi.org/10.1002/chin.199147192
https://doi.org/10.1002/chin.199147192
Publikováno v:
ChemInform. 30
The synthesis of three thiophene analogues of Flosulide – a potent and selective inhibitor of cyclooxygenase subtype 2 (COX-2) – is described. Utilizing combined Friedel-Crafts acylation and alkylation of 2-chlorothiophene, simplified procedures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::deb4bd05db0c3e61eab98916424139a7
https://doi.org/10.1002/chin.199901122
https://doi.org/10.1002/chin.199901122
Publikováno v:
ChemInform. 30
Three isomeric substituted thienoimidazothiazoles were synthesized as thiophene analogs of the immune modulator TILOMISOL, by cyclizing appropriate β-oxothioethers of thienoimidazoles. In contrast to the benzene analog no intermediates were observed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3c3fbc649e55b794dac859f6865eed8
https://doi.org/10.1002/chin.199904130
https://doi.org/10.1002/chin.199904130