Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Margriet Ovaere"'
Autor:
Mateusz Rebarz, Margriet Ovaere, Andrée Kirsch-De Mesmaeker, Cécile Moucheron, Wim Dehaen, Luc Van Meervelt, Leen L. Volker, David Beljonne, Diane Ramlot
Publikováno v:
European Journal of Inorganic Chemistry. 2013:2031-2040
Rh and Ir complexes that contain meso-(p-methoxyphenyl)dipyrromethene (dipy) and phenylpyridine (ppy) ligands {i.e., [Rh(dipy)3], [Rh(ppy)2(dipy)] and [Ir(ppy)2(dipy)]} have been prepared and their electrochemical and luminescence behaviour are discu
Publikováno v:
Nucleic Acids Research
Altritol nucleic acids (ANAs) are a promising new tool in the development of artificial small interfering ribonucleic acids (siRNAs) for therapeutical applications. To mimic the siRNA:messenger RNA (mRNA) interactions, the crystal structure of the AN
Publikováno v:
Chemistry – A European Journal. 17:7823-7830
Cyclohexenyl nucleic acids (CeNA) are characterised by the carbon-carbon double bond replacing the O4'-oxygen atom of the natural D-2'-deoxyribose sugar ring in DNA. CeNAs exhibit a high conformational flexibility, are stable against nuclease activit
Autor:
Margriet Ovaere, Frans Compernolle, Jo Nelissen, Wim M. De Borggraeve, An Van den Bogaert, Luc Van Meervelt
Publikováno v:
European Journal of Organic Chemistry. 2010:5397-5401
Benzodiazepines show a broad spectrum of biological activities. In an ongoing effort to extend molecular diversity in this type of systems, we developed a strategy for synthesizing 3,4-dihydro-1H-pyrido[2,3-e][1,4]diazepine-2,5-dione compounds starti
Autor:
Wim Dehaen, Luc Van Meervelt, Margriet Ovaere, Koen Robeyns, Wouter Maes, Joice Thomas, Mario Smet
Publikováno v:
Organic Letters. 11:3040-3043
A novel family of homoselenacalix[n]arenes (n = 3-8), with bridging CH(2)SeCH(2) groups connecting the aryl subunits, has been synthesized via two different approaches employing nucleophilic Se species. The macrocycles are adequately characterized, i
Publikováno v:
Organic Letters. 11:1681-1684
The first rational, stepwise synthesis of enlarged oxacalix[n]arenes (n > 4) is described. Variously substituted oxacalix[3]arene[3]pyrimidines were prepared rather selectively by a straightforward [3 + 3] fragment coupling approach after a thorough
Autor:
Margriet Ovaere, Luc Van Meervelt, Frans Compernolle, Wim M. De Borggraeve, An Van den Bogaert, Jo Nelissen
Publikováno v:
ChemInform. 42
Synthesis of the title compounds is achieved using the Ugi multicomponent reaction as key step.
Publikováno v:
Organic letters. 13(1)
The critical synthetic access to odd-numbered calix[n]arenes has evidently resulted in less attention for these macrocycles, although specific molecular recognition phenomena have been observed for some of them. A straightforward fragment coupling ap
Publikováno v:
Acta crystallographica. Section F, Structural biology and crystallization communications. 66(Pt 4)
In altritol nucleic acids (ANAs), the natural five-membered ribose ring of RNA is replaced by the six-membered D-altritol ring. ANAs are good candidates to act as siRNAs in the RNA-interference pathway. Crystals of the fully modified altritol self-co
Publikováno v:
ChemInform. 39
Diversely functionalized oxacalix[2]arene[2]pyrimidines have been synthesized starting from a bis(methylsulfanyl)-substituted oxacalix[4]arene by two efficient post-macrocyclization pathways. Functionalized aryl groups were introduced on the pyrimidi