Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Steven L. Cappelle"'
Autor:
Georges J. Hoornaert, Ilse A. Vogels, Steven L. Cappelle, Frans Compernolle, Suzanne Toppet, Tom C Govaerts
Publikováno v:
Tetrahedron. 58:3655-3666
An efficient route has been developed for the synthesis of polysubstituted 6,6-dioxo-6,7-dihydrothieno[3,4- b ]pyridines 3 , which serve as excellent precursors for generation of the corresponding pyridine o -quinodimethanes. Following thermal extrus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa0c07da0ad45f9aa4d919049ae81515
https://doi.org/10.1016/s0040-4020(02)00348-4
https://doi.org/10.1016/s0040-4020(02)00348-4
Autor:
Georges J. Hoornaert, Steven L. Cappelle, Frans Compernolle, Ilse A. Vogels, Luc Van Meervelt
Publikováno v:
Tetrahedron Letters. 42:3759-3762
An efficient route has been developed for the synthesis of polysubstituted 6,6-dioxo-6,7-dihydrothieno[3,4-b]pyridine 5 . This pyridine sulfolene compound serves as an excellent precursor for the corresponding pyridine o-quinodimethane. This reactive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15b498033034ce8fe3f65d1095899b1c
https://doi.org/10.1016/s0040-4039(01)00566-4
https://doi.org/10.1016/s0040-4039(01)00566-4
Publikováno v:
Tetrahedron. 57:4203-4212
Various pyridine o -quinodimethane systems were generated via thermal extrusion of sulfur dioxide from 1,3-dihydro-2,2-dioxothieno[3,4- c ]pyridine precursors and derivatives functionalised in the 1- or 3-position of the sulfolene ring moiety. Depend
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f07f981bc13cb1d69e9b5bb73dad2bb7
https://doi.org/10.1016/s0040-4020(01)00289-7
https://doi.org/10.1016/s0040-4020(01)00289-7
Publikováno v:
Tetrahedron. 52:11889-11904
The polyfunctional 2,3- and 3,4-o-bis(chloromethyl)pyridines 3, produced via cycloaddition of the oxazinones 2 with propargyl chloride and 1,4-dichloro-2-butyne, were used as precursors of various pyridine o-quinodimethane analogues. The 2,3- and 3,4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40d37f6eff3417693d85f7951b1760d4
https://doi.org/10.1016/0040-4020(96)00680-1
https://doi.org/10.1016/0040-4020(96)00680-1
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b14497a17b637677b387182aeeae90c
https://doi.org/10.1002/chin.199701183
https://doi.org/10.1002/chin.199701183
Publikováno v:
ChemInform. 32
Various pyridine o -quinodimethane systems were generated via thermal extrusion of sulfur dioxide from 1,3-dihydro-2,2-dioxothieno[3,4- c ]pyridine precursors and derivatives functionalised in the 1- or 3-position of the sulfolene ring moiety. Depend
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5390cbd6cb3c8a545d9bc829c979724
https://doi.org/10.1002/chin.200134038
https://doi.org/10.1002/chin.200134038
Autor:
Ilse A. Vogels, Luc Van Meervelt, Steven L. Cappelle, Frans Compernolle, Georges J. Hoornaert
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f69d85a2634e842e128e1073cf2d3b6
https://doi.org/10.1002/chin.200136138
https://doi.org/10.1002/chin.200136138
Autor:
Frans Compernolle, Tom C Govaerts, Georges J. Hoornaert, Suzanne Toppet, Steven L. Cappelle, Ilse A. Vogels
Publikováno v:
ChemInform. 33
An efficient route has been developed for the synthesis of polysubstituted 6,6-dioxo-6,7-dihydrothieno[3,4- b ]pyridines 3 , which serve as excellent precursors for generation of the corresponding pyridine o -quinodimethanes. Following thermal extrus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3cd064f5c388e01064d48488fa2e2c90
https://doi.org/10.1002/chin.200240155
https://doi.org/10.1002/chin.200240155