Zobrazeno 1 - 8
of 8
pro vyhledávání: '"W. ROGER TULLY"'
Publikováno v:
Tetrahedron Letters. 33:551-554
The synthesis of phospholipid analogues, designed to show a novel made of phospholipase A 2 inhibition, is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7170168751775b01df2c2c6f13d87426
https://doi.org/10.1016/s0040-4039(00)93993-5
https://doi.org/10.1016/s0040-4039(00)93993-5
Publikováno v:
Drug Development Research. 22:299-308
The observation that the imidazoquinoxaline ethyl ester RU32180 possessed an affinity of 175 nM for benzodiazepine (BDZ) receptors led to the discovery of several series of potent receptor ligands such as esters ofimidazoquinolines and imidazobenzoth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f6de5440be2ff507024920d4563825f
https://doi.org/10.1002/ddr.430220402
https://doi.org/10.1002/ddr.430220402
Synthesis of (imidazo[1,2-C]pyrimidin-2-yl)phenylmethanones and 6-benzoylpyrrolo[2,3-D]pyrimidinones
Publikováno v:
Journal of Heterocyclic Chemistry. 26:293-299
4-Pyrimidinamines have been reacted with 3-bromo-1-phenylpropane-1,2-dione to give a series of (imidazo[1,2-c]pyrimidin-2-yl)phenylmethanones. The dione also reacted with ethyl amidinoacetate to yield ethyl 2-amino-5-benzoylpyrrole-2-carboxylate whic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4163396349b4e8e0b3deddb3ad91f05
https://doi.org/10.1002/jhet.5570260206
https://doi.org/10.1002/jhet.5570260206
Publikováno v:
Journal of Heterocyclic Chemistry. 23:833-841
4-Quinazolinones have been cyclised to [1,2,4]triazoloquinazolinones and to imidazoquinazolinones. The direction of cyclisation has been proved by the unambiguous synthesis of their ethylation products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df95201cd33fc0bf81f2a3c9c3be2f88
https://doi.org/10.1002/jhet.5570230335
https://doi.org/10.1002/jhet.5570230335
Autor:
JOHN B. TAYLOR, W. ROGER TULLY
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f49052d79f697aa2b7790d716a0cb6c4
https://doi.org/10.1002/chin.197638282
https://doi.org/10.1002/chin.197638282
Autor:
John B. Taylor, W. Roger Tully
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1331
The synthesis of 3,4-dihydro-1H-1,3-benzodiazepine-2,5-dione has been carried out, and the reactivity at positions 2, 5, and 7 investigated. Attempts to introduce a 4,5-double bond resulted in rearrangement to quinolines and indoles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77831d30d179ef9429eef247c090fe99
https://doi.org/10.1039/p19760001331
https://doi.org/10.1039/p19760001331
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.