Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Adolphe Waefelaer"'
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 85:898-903
Several new 5‐aryl‐2,3,4,5‐tetrahydrobenzo[f]1,4‐oxazepine derivatives (1 to 18) were prepared by reduction of the 2,3‐dihydro compounds. Adams platinium was a suitable catalyst for hydrogenation. With other catalysts, reduction of a nitro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36b77aa78e95e0d814c8a600428f4f37
https://doi.org/10.1002/bscb.19760851108
https://doi.org/10.1002/bscb.19760851108
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 85:421-425
Several new phenoxyalkylamines (8 to 17) were obtained either by reductive ammonolysis of phenoxyalkanones (2), by reduction of phenoxycyanoalkanes (4), by reduction of oximes (3) or by the application of the Gabriel reaction of phenoxyhalogenoethane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c479fb30f206c2e4f03e4811eadbf1d7
https://doi.org/10.1002/bscb.19760850606
https://doi.org/10.1002/bscb.19760850606
Autor:
Jacques Pecher, Adolphe Waefelaer
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 87:911-915
The 3‐(3,4‐dimethoxyphenoxyalkylamino) phthalides (4) cyclize in PPA solution to demethylated and demethoxylated 2,3‐dihydro‐8‐oxo‐anthraceno [9, 9a, 1‐ef] 1,4‐oxazepines (7) as well as to 6,7,9,13b‐tetrahydro‐9‐oxo‐benzo [a]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e45059c7c621c170a36fae737908f6ac
https://doi.org/10.1002/bscb.19780871113
https://doi.org/10.1002/bscb.19780871113
Autor:
Didier Francart, Robert René Smolders, Jean Hanuise, Roland Coomans, Adolphe Waefelaer, Nicole Voglet
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 91:33-42
A partir des 5-, 6- et 7-fluoroisatines, on decrit la synthese des 9-, 10- et 11-fluoroacronycines via les 5-, 6- et 7-fluoro-1,3-dihydroxy-10-methylacridan-9-ones. An unambiguous synthesis of 9-, 10- and 11-fluoroacronycines is described starting fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26775b9c1a4ee9e344900fcbda022569
https://doi.org/10.1002/bscb.19820910105
https://doi.org/10.1002/bscb.19820910105
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 85:787-793
Several new 5‐aryl‐2,3‐dihydrobenzo [f] 1,4‐oxazepine derivatives (10) to 25) were obtained in high yields by cyclodehydration of N‐phenoxyalkylbenzamides derivatives (26 to 41). Copyright © 1976 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinhei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f97c9260873f453b00b2c34107bf2c28
https://doi.org/10.1002/bscb.19760851008
https://doi.org/10.1002/bscb.19760851008
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 86:1003-1007
The condensation of 2‐aryloxyalkylamines (1) with 2‐formylbenzoic acid gives substituted aminophthalides (8) which can be isolated in some cases and which cyclize to benzo [a] 1,4‐oxazepino [5,4‐a]isoindoles (11) 2‐(3, 4‐Dimethoxyphenoxy)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f53715f4972509922fb8b0593611a975
https://doi.org/10.1002/bscb.19770861211
https://doi.org/10.1002/bscb.19770861211
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8651ec37e93f381edeebb9c5c8e71e06
https://doi.org/10.1002/chin.198222328
https://doi.org/10.1002/chin.198222328
Publikováno v:
Chemischer Informationsdienst. 9
The condensation of 2‐aryloxyalkylamines (1) with 2‐formylbenzoic acid gives substituted aminophthalides (8) which can be isolated in some cases and which cyclize to benzo [a] 1,4‐oxazepino [5,4‐a]isoindoles (11) 2‐(3, 4‐Dimethoxyphenoxy)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ec2c2df005f0af8e025f76ed6bee91f
https://doi.org/10.1002/chin.197818273
https://doi.org/10.1002/chin.197818273
Autor:
Jacques Pecher, Adolphe Waefelaer
Publikováno v:
Chemischer Informationsdienst. 10
The 3‐(3,4‐dimethoxyphenoxyalkylamino) phthalides (4) cyclize in PPA solution to demethylated and demethoxylated 2,3‐dihydro‐8‐oxo‐anthraceno [9, 9a, 1‐ef] 1,4‐oxazepines (7) as well as to 6,7,9,13b‐tetrahydro‐9‐oxo‐benzo [a]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7684cabbd7f9fd5c7130a0a4a2d798c2
https://doi.org/10.1002/chin.197926291
https://doi.org/10.1002/chin.197926291