Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ilse A. Vogels"'
Autor:
J. Emanuel Ramos de Carvalho, Milan T. Verwoert, Ilse M.C. Vogels, Eric A. Reits, Cornelis J.F. Van Noorden, Ingeborg Klaassen, Reinier O. Schlingemann
Publikováno v:
Biochemistry and Biophysics Reports, Vol 13, Iss , Pp 83-92 (2018)
Emerging evidence suggests that dysfunction of the ubiquitin-proteasome system is involved in the pathogenesis of numerous senile degenerative diseases including retinal disorders. The aim of this study was to assess whether there is a link between p
Externí odkaz:
https://doaj.org/article/73e3bd5ff407494f882b26db49836d2f
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
Publikováno v:
Tetrahedron Letters. 43:799-802
2(1H)-Pyrazinones were converted into [3,4-b] and [3,4-c] sulfolene pyridinones 4 and 5, serving as precursors for the corresponding 3,4- and 5,6-dimethylene 2(1H)-pyridinone ortho-quinodimethanes. These were trapped by in situ reaction with dienophi
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
Autor:
Ilse A. Vogels, Luc Van Meervelt, Steven L. Cappelle, Frans Compernolle, Georges J. Hoornaert
Publikováno v:
ChemInform. 32
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
Publikováno v:
ChemInform. 35
2(1H)-Pyrazinones were converted into various [3,4-b] sulfolene pyridinones 19–21 , serving as precursors for thermolytic conversion into the corresponding 5,6-dimethylene 2(1H)-pyridinone ortho-quinodimethanes. These were trapped in situ by reacti
Publikováno v:
ChemInform. 34
1-Benzyl-3-(bromomethyl)-2(1 H )-pyrazinone was converted to [3,4- c ] sulfolene pyridinone 8a and further (1- or 3-) substituted derivatives having a dienophilic side chain on the sulfolene ring. Thermolytic extrusion of sulfur dioxide from o -QDM p