Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Fokke Venema"'
Autor:
Dianne van Strijp, Fokke Venema, Carine Zintilini, Corinne Jay, Paul van de Wiel, Birgit Deiman, Saskia Vermeer
Publikováno v:
Journal of Virological Methods. 151:283-293
A new mechanism is described for DNA amplification using nucleic acid sequence-based amplification (NASBA) including a restriction enzyme digestion and P1 primer binding directly upstream of the digestion. For hepatitis B virus (HBV), herpes simplex
Autor:
Martinus C. Feiters, Fokke Venema, Roeland J. M. Nolte, Patrick Berthault, Alan E. Rowan, Nicolaos Birlirakis, Hubertus F. M. Nelissen
Publikováno v:
Chemistry - A European Journal. 4:2237-2250
The synthesis of homo- and heterocyclodextrin (CD) dimers, containing two CD moieties that are linked through their secondary sides by alipathic or 2,2'-bipyridyl spacers is described. In these dimers, the glucose units to which the spacers are linke
Publikováno v:
Tetrahedron. 54:3513-3522
The unusual conformational behaviour of a series of new cyclodextrin (CD) dimers is studied by dedicated 1H-NMR techniques. In water some CD-dimers form stable self-inclusion complexes, for which the aliphatic linker is partially included in one of t
Autor:
Martinus C. Feiters, Fokke Venema, Hubertus F. M. Nelissen, Roeland J. M. Nolte, René M. Uittenbogaard
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :2045-2053
The synthesis of three dansyl appended cyclodextrin derivatives, differing in the spacer length between cyclodextrin and the dansyl moiety, is described. In compound 4 the fluorophore is directly attached to the cyclodextrin. Compound 5 contains an e
Publikováno v:
Tetrahedron Letters. 35:8661-8664
The synthesis of two novel cyclodextrin heterodimers derived from α- and β-cyclodextrin is reported. The cyclodextrin molecules are linked via alkyl spacers on their secondary sides. NMR-studies indicate that the spacer is bound in one of the two c
Autor:
Martinus C. Feiters, David N. Reinhoudt, Erik van Dienst, Chantal M. Baselier, Johannes F.J. Engbersen, Bianca H.M. Ruel, Roeland J. M. Nolte, Fokke Venema
Publikováno v:
Tetrahedron letters, 35(11), 1773-1776. Elsevier
The synthesis of three cyclodextrin dimers from the novel building block 3-amino-3-deoxy-heptakis(6-O-tert-butyldimethylsilyl)-ß-cyclodextrin is reported. The cyclodextrins are linked with an amide bond on their secondary sides to an ethylene, octam
Autor:
Martinus C. Feiters, David N. Reinhoudt, Bianca H.M. Ruel, Chantal M. Baselier, Johannes F.J. Engbersen, E.S. van Dienst, Fokke Venema, Roeland J. M. Nolte
Publikováno v:
ChemInform. 25
Autor:
Roeland J. M. Nolte, Nicolaos Birlirakis, Fokke Venema, Martinus C. Feiters, Alan E. Rowan, Patrick Berthault, Hubertus F. M. Nelissen
Publikováno v:
ChemInform. 30
The synthesis of homo- and heterocyclodextrin (CD) dimers, containing two CD moieties that are linked through their secondary sides by alipathic or 2,2'-bipyridyl spacers is described. In these dimers, the glucose units to which the spacers are linke
Autor:
Roeland J. M. Nolte, Fokke Venema, Martinus C. Feiters, Hubertus F. M. Nelissen, Menno R. de Jong
Publikováno v:
Sensor Technology in the Netherlands: State of the Art ISBN: 9789401061032
Cyclodextrins (CDs), which bind organic substrates in their cavities, can be used to give mass sensitive sensor devices a selective coating. We have tested this principle for the detection of toluene vapour by a Quartz Crystal Mircrobalance (QMB) wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6607d030cdc6055734628c0edd0aaf88
https://doi.org/10.1007/978-94-011-5010-1_35
https://doi.org/10.1007/978-94-011-5010-1_35
Autor:
Martinus C. Feiters, Arnoldus F. J. Schut, Hubertus F. M. Nelissen, Roeland J. M. Nolte, Fokke Venema
Publikováno v:
Chemical Communications. :577-578
A luminescent ruthenium(II) complex with six cyclodextrin binding sites is shown to switch off its emission upon binding of N,N′-dinonyl-4,4′-bipyridinium bromide and to recover luminescence upon displacement of the bipyridinium ion by a steroid.