Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Daniel Lamar Zabrowski"'
Publikováno v:
Tetrahedron. 53:1-20
The amino azanoradamantane hexahydro-2,5b-methano-IH-3aS,3aa,6aa-cyclopenta-[clpyrrole-4a-amine 1 and the corresponding enantiomer ent-1 have been prepared along with benzamide derivatives SC-52491 and SC-52490, respectively, which are of pharmaceuti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af0813e8e81b6ccceecb91b2f76f57fd
https://doi.org/10.1016/s0040-4020(96)00973-8
https://doi.org/10.1016/s0040-4020(96)00973-8
Publikováno v:
ChemInform. 24
Methyl 2-iodo-2-(phenylsulfonyl)-4-pentenoate ( 8 )is reacted with N-BOC-allylamine to afford substituted 3-azabicyclo-[3.3.0]octanes ( 10 ) in a process which involves an initial iodine atom-transfer annulation followed by an ionic cyclization. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac8a43c63f764b8401883530e61343e0
https://doi.org/10.1002/chin.199316178
https://doi.org/10.1002/chin.199316178
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17c9710d295bb0f2ae4097c91aaa01f0
https://doi.org/10.1002/chin.199316202
https://doi.org/10.1002/chin.199316202
Publikováno v:
ChemInform. 28
The amino azanoradamantane hexahydro-2,5b-methano-IH-3aS,3aa,6aa-cyclopenta-[clpyrrole-4a-amine 1 and the corresponding enantiomer ent-1 have been prepared along with benzamide derivatives SC-52491 and SC-52490, respectively, which are of pharmaceuti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d224bbf3942d0c295dbebecf83ba028b
https://doi.org/10.1002/chin.199714124
https://doi.org/10.1002/chin.199714124
Publikováno v:
Tetrahedron Letters. 33:7283-7286
A route to azanoradamantanes is described which makes use of an atom-transfer radical cyclization to afford 3-azabicyclo[3.3.0]octanes 3A and 3B . Subsequent elaboration of exo-allylamine functionality, followed by cyclization of the endo-hydroxymeth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::872b62a639ed89b03a4ce683d161d6e4
https://doi.org/10.1016/s0040-4039(00)60166-1
https://doi.org/10.1016/s0040-4039(00)60166-1
Autor:
Daniel L. Flynn, Gary W. Gullikson, Roger Nosal, Dai C. Yang, Daniel Lamar Zabrowski, Daniel P. Becker, Chafiq Moummi, Clara I. Villamil
Publikováno v:
Journal of Medicinal Chemistry. 35:1486-1489
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3639941cbf94a1833d4761d48f2eeaf0
https://doi.org/10.1021/jm00086a019
https://doi.org/10.1021/jm00086a019
Publikováno v:
ChemInform. 21
Iodomalonate-mediated atom-transfer annulations can be performed to give azacyclic systems, provided the nucleophilic character of the allylamine is low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32492628e7462d500d581106762905b0
https://doi.org/10.1002/chin.199043163
https://doi.org/10.1002/chin.199043163
Publikováno v:
Tetrahedron Letters. 33:7281-7282
Methyl 2-iodo-2-(phenylsulfonyl)-4-pentenoate ( 8 )is reacted with N-BOC-allylamine to afford substituted 3-azabicyclo-[3.3.0]octanes ( 10 ) in a process which involves an initial iodine atom-transfer annulation followed by an ionic cyclization. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e21e83eb87d7bdbb35e320495e26f596
https://doi.org/10.1016/s0040-4039(00)60165-x
https://doi.org/10.1016/s0040-4039(00)60165-x
Publikováno v:
The Journal of Organic Chemistry. 55:3673-3674
Iodomalonate-mediated atom-transfer annulations can be performed to give azacyclic systems, provided the nucleophilic character of the allylamine is low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cb9e986f80cfcfcbc53f89533a5c058
https://doi.org/10.1021/jo00298a058
https://doi.org/10.1021/jo00298a058
Publikováno v:
Tetrahedron Letters. 29:4501-4504
The oxidation of aromatic amines to the corresponding nitro substituents is performed under mild, nonacidic conditions in the presence of highly nucleophilic aromatic systems such as indoles and furans.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd9ce7fe4853e396d5d764215e32fb7e
https://doi.org/10.1016/s0040-4039(00)80531-6
https://doi.org/10.1016/s0040-4039(00)80531-6