Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Fokke Venema"'
Autor:
Werts MH; Laboratory of Organic Chemistry University of Amsterdam Nieuwe Achtergracht 129, 1018 WS Amsterdam (The Netherlands)., Woudenberg RH, Emmerink PG, van Gassel R, Hofstraat JW, Verhoeven JW
Publikováno v:
Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2000 Dec 15; Vol. 39 (24), pp. 4542-4544.
Autor:
Werts, Martinus H. V., Woudenberg, Richard H., Emmerink, Peter G., Gassel, Rob van, Hofstraat, Johannes W., Verhoeven, Jan W.
Publikováno v:
Angewandte Chemie. International Edition; December 15, 2000, Vol. 39 Issue: 24 p4542-4544, 3p
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