Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Gabor Blasko"'
Publikováno v:
Synlett. 2010:2411-2414
Novel 2-benzazepino[4,5-a]naphthalene derivatives were synthesised efficiently via 1,7-electrocyclisation of nonstabilised azomethine ylides derived from 1-aryl- or 1-alkenyl-naphthalene-2-carbaldehyde derivatives. In some cases, surprisingly, pyrrol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::757f02531f2218c9da4828d955fd983e
https://doi.org/10.1055/s-0030-1258036
https://doi.org/10.1055/s-0030-1258036
Publikováno v:
ChemInform. 46
A novel cascade condensation-intramolecular acylation process for the synthesis of the title compounds from anthranilic acid derivatives is developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a1d91420620cb2970f1c2160ddf3983
https://doi.org/10.1002/chin.201541203
https://doi.org/10.1002/chin.201541203
Publikováno v:
Tetrahedron Letters. 46:6927-6930
New reactions of 6,7-dimethoxy-3,4-dihydroisoquinoline and 3,4-dihydro-β-carboline with various electron-deficient olefins are described. ‘One-pot’ generation and cycloaddition of the 1,3- and 1,4-dipoles formed from these heterocycles with a ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::945b8628e15eac1e750c186ce5ca151a
https://doi.org/10.1016/j.tetlet.2005.08.006
https://doi.org/10.1016/j.tetlet.2005.08.006
Publikováno v:
Synthesis. 2005:2039-2045
A simple one-pot process for the alkylation of isoquino-lines followed by a dehydrohalogenation of the quaternary salts formed and by an in situ trapping of azomethine ylides with appropriate dipolarophiles is described. This method has successfully
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6658abcfc22babe2684b91cc5a9bf0a5
https://doi.org/10.1055/s-2005-869908
https://doi.org/10.1055/s-2005-869908
The reaction of various anthranilic acid derivatives or their esters with 4-oxotetrahydrothiophene-3-carbonitrile 2, 2-oxocyclopentanecarbonitrile (9, n = 1) or 2-oxocyclohexanecarbonitrile (9, n = 2) in ethanol under reflux conditions giving rise th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5cd37038ed3cb0c07270a32a54ded26
Autor:
Miklos Nyerges, Imre Fejes, Gabor Blasko, Françoise Perron-Sierra, Tibor Novák, Eszter Graczol‐Foerdoes
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9fe8b78825888364b9c17f88d622888
https://doi.org/10.1002/chin.201409161
https://doi.org/10.1002/chin.201409161
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0736dea7ff9de1bdd7e753fa86b55c5b
https://doi.org/10.1002/chin.200123102
https://doi.org/10.1002/chin.200123102
Publikováno v:
ChemInform. 41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28591681ddd28ae23d2d36b331be2bfe
https://doi.org/10.1002/chin.201018147
https://doi.org/10.1002/chin.201018147
Publikováno v:
ChemInform. 40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed0f96f205bd1f0d02d21aef0a26d863
https://doi.org/10.1002/chin.200951169
https://doi.org/10.1002/chin.200951169
Publikováno v:
Synthesis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f0db9d7fd8857936a30a094f44eed54
https://doi.org/10.1055/s-0029-1217063
https://doi.org/10.1055/s-0029-1217063