Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jean-Marc Girodeau"'
Autor:
R. M. Mcmillan, Pierre Andre Raymond Bruneau, John F. Kingston, T. Geoffrey C. Bird, Graham Charles Crawley, Martin Paul Edwards, Jean Marc Girodeau, S. J. Foster
Publikováno v:
Journal of medicinal chemistry. 34(7)
(Methoxyalkyl)thiazoles are novel 5-lipoxygenase (5-LPO) inhibitors that are neither redox agents nor iron chelators. Consideration of a hypothetical model of the enzyme active site led to this series which is exemplified by 1-[3-(naphth-2-ylmethoxy)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50f059b5864a3c875d21a2932bceb544
https://pubmed.ncbi.nlm.nih.gov/1648621
https://pubmed.ncbi.nlm.nih.gov/1648621
Publikováno v:
Helvetica Chimica Acta. 63:2096-2111
A number of functionalized and chiral macrocyclic polyethers have been synthesized by condensation of the dithallium alcoholate of (R,R)-(+)-tartaric acid derivatives with α, ω-dihalides. In this way for instance, the tetracarboxylic [18]-O6 macroc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c85092b76e81b46bb264244c6b45a22b
https://doi.org/10.1002/hlca.19800630736
https://doi.org/10.1002/hlca.19800630736
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e242fbee32ffeaac1a100daf5df917a
https://doi.org/10.1002/chin.198643119
https://doi.org/10.1002/chin.198643119
Publikováno v:
The Journal of antibiotics. 37(2)
Lividamine and paromamine were converted into two key intermediate ethylenic aldehydes 10a and 10b. Reductive amination of the two aldehydes yielded the protected sisamine 11a and the three analogs 11b, 12a and 12b. These four derivatives were deprot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91672bf16cb87ccecf43082e3bdba1e2
https://pubmed.ncbi.nlm.nih.gov/6546750
https://pubmed.ncbi.nlm.nih.gov/6546750
Publikováno v:
Chemischer Informationsdienst. 12
Das Di-Tl-Salz (Ib) des (R,R)-Weinsaurediamids (Ia) reagiert mit dem Diiodid (II) unter Bildung des makrocyclischen Polyethers (IIIa) (daneben wenig des Trimeren (IV)); analog wird aus dem Bisamid (Ic) uber (Id) mit (II) das Analoge (IIIb) erhalten.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba055eb4fd78106e2269657c05b4278e
https://doi.org/10.1002/chin.198106270
https://doi.org/10.1002/chin.198106270
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a1e198c709e60f56acaddb4433744ae
https://doi.org/10.1002/chin.197604217
https://doi.org/10.1002/chin.197604217
Publikováno v:
Angewandte Chemie. 87:813-814
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9502ef2c987fcbcf42e6e5f17733d34
https://doi.org/10.1002/ange.19750872210
https://doi.org/10.1002/ange.19750872210
Publikováno v:
Angewandte Chemie International Edition in English. 14:764-764
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eb64869f59a77f0761ab61fe898656c
https://doi.org/10.1002/anie.197507641
https://doi.org/10.1002/anie.197507641