Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Eileen B. Walsh"'
Publikováno v:
Tetrahedron Letters. 29:4401-4404
6-[(Dimethylamino)methylene]amino-1,3-dimethyluracil 1 undergoes formal [4+2] cycloaddition reactions with electron deficient olefins to give pyrido[2,3-d]pyrimidines. With DMAD or azodicarboxylates Michael addition occurs leading to pyrrolo[3,4-c]py
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa384855d4dd166deb4296f5590308eb
https://doi.org/10.1016/s0040-4039(00)80505-5
https://doi.org/10.1016/s0040-4039(00)80505-5
Publikováno v:
The Journal of Organic Chemistry. 51:2011-2021
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d16313479ec956a9e377bbe6f360b98
https://doi.org/10.1021/jo00361a014
https://doi.org/10.1021/jo00361a014
Publikováno v:
The Journal of Organic Chemistry. 52:2285-2292
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8855350985e00974e7638f3acaef4d8
https://doi.org/10.1021/jo00387a032
https://doi.org/10.1021/jo00387a032
Autor:
Heinrich Wamhoff, Eileen B. Walsh
Publikováno v:
Chemische Berichte. 122:1673-1679
Electron-rich 6-vinyl- and 6-(azavinyl)pyrimidinediones, such as 6-{[(dimethylamino)methylene]amino}- (1) and 6-[2-(dimethyl-amino)vinyl]-1,3-dimethyl-2,4(1H,3H)-pyrimidinediones (8), undergo cycloaddition reactions with electron deficient olefins to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca8dab813f450082708f25f7773739d5
https://doi.org/10.1002/cber.19891220913
https://doi.org/10.1002/cber.19891220913
Autor:
Eileen B. Walsh, Kevin T. Potts
Publikováno v:
The Journal of Organic Chemistry. 53:1199-1202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1cb69b0cff1ef443723d67e33c0a8fc
https://doi.org/10.1021/jo00241a014
https://doi.org/10.1021/jo00241a014
Publikováno v:
J. Chem. Soc., Chem. Commun.. :114-116
Quinoline- and isoquinoline-5,8-diones react with 1-methoxycyclohexa-1,3-diene at 80 °C, the former giving 8-methoxy-1-aza-anthraquinone regiospecifically and the latter 5-methoxy-2-aza-anthraquinone regioselectively; in similar cycloadditions, subs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a96cb4e007cc4dcd6630fc22c70fb54
https://doi.org/10.1039/c39840000114
https://doi.org/10.1039/c39840000114
Autor:
Kevin T. Potts, Eileen B. Walsh
Publikováno v:
The Journal of Organic Chemistry. 49:4099-4101
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f48df0791986711ecdab5c5a696a60fc
https://doi.org/10.1021/jo00195a058
https://doi.org/10.1021/jo00195a058
Autor:
Eileen B. Walsh, Kevin T. Potts
Publikováno v:
Chemischer Informationsdienst. 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04338e93ff08912d1f30f93acd92727a
https://doi.org/10.1002/chin.198516113
https://doi.org/10.1002/chin.198516113
Publikováno v:
Journal of the Chemical Society, Chemical Communications; 1/15/1984, Issue 2, p114-116, 3p