Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marianne R. Spada"'
Publikováno v:
Journal of Heterocyclic Chemistry. 26:1851-1857
The utility of certain 5-alkynyloxy-, 5-alkynylthio, and 5-alkynylsulfinyl-pyrimidines as precursors of 7-substituted furo[3,2-d]- and thieno[3,2-d]pyrimidines has been examined. When treated with sodium methoxide in warm methyl sulfoxide, 1,3-dimeth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4361c5e4f1ac1a010554108b0b10b2ce
https://doi.org/10.1002/jhet.5570260659
https://doi.org/10.1002/jhet.5570260659
Publikováno v:
Nucleosides and Nucleotides. 16:1983-1998
Two approaches to the synthesis of the title compounds are described. In the first route, a reactive 5-oxo-6-methylene pyrimidine intermediate that is generated by treating the bis-acetylated or bis-benzoylated nucleosides 10 and 11 with sodium hydro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::081a49282bc1d7d857074ac232fc6d3b
https://doi.org/10.1080/07328319708002549
https://doi.org/10.1080/07328319708002549
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d7281456f0eebd984e11aa4fe48e39b
https://doi.org/10.1002/chin.199815239
https://doi.org/10.1002/chin.199815239
Autor:
Akira Matsuda, Linda A. Jelicks, Brian A. Otter, Marianne R. Spada, Robyn S. Klein, Yuichi Yoshimura, Shirish A. Patil
Publikováno v:
Nucleosides and Nucleotides. 11:615-635
The 5-oxo-6-methylene-pyrimidine-2,4-dione intermediate (6) that is formed when 5-acetoxy-6-acetoxymethyl-1-β-D-(5-O-acetyl-2,3-O-isopropylidene)-ribofuranosyluracil (5) is treated with sodium hydroxide undergoes cyclization at pH 14 to give 2′,3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57825bbd075a6ad5a998e109c5ba119f
https://doi.org/10.1080/07328319208021730
https://doi.org/10.1080/07328319208021730
Publikováno v:
European journal of pharmacology. 266(1)
The present study was undertaken to characterize [3H]ifenprodil binding in rat brain. [3H]Ifenprodil showed saturable, high-affinity binding at 4 degrees C. Specific binding, defined with 10 microM ifenprodil as a competitor, was inhibited biphasical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b17efe20f3d40911efc82cfddf48b2e5
https://pubmed.ncbi.nlm.nih.gov/7907988
https://pubmed.ncbi.nlm.nih.gov/7907988
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34c42fdce6ba84057c7551004b8dba75
https://doi.org/10.1002/chin.199022193
https://doi.org/10.1002/chin.199022193