Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Weemers, J.J.M."'
Autor:
Weemers, J.J.M., Wiecko, J., Pidko, E.A., Weber, M., Lutz, M., Müller, Christian, Crystal and Structural Chemistry, Sub Crystal and Structural Chemistry
Publikováno v:
Chemistry : A European Journal, 19(43), 14458-14469. Wiley-VCH Verlag
Chemistry-A European Journal, 19(43), 14458. Wiley
Chemistry-A European Journal, 19(43), 14458. Wiley
The novel atropisomeric pyridine derivative rac-10 has been synthesized and structurally characterized. In contrast to its phosphorus analogue 3, axially chiral 10 has a considerably lower rotational barrier as estimated by DFT calculations. However,
Autor:
Campos-Carrasco, A., Broeckx, L.E.E., Weemers, J.J.M., Pidko, E.A., Lutz, M., Masdeu-Bultó, A. M., Vogt, D., Müller, Christian, Rontgen participation programme, Sub Crystal and Structural Chemistry
Publikováno v:
Chemistry : A European Journal, 17(8), 2510-2517. Wiley-VCH Verlag
Chemistry-A European Journal, 17(8), 2510. Wiley
Chemistry-A European Journal, 17(8), 2510. Wiley
The coordination chemistry of the bidentate P,N hybrid ligand 2- (2’-pyridyl)-4,6-diphenylphosphinine (1) towards PdII and PtII has been investigated. The molecular structures of the complexes [PdCl2(1)] and [PtCl2(1)] were determined by X-ray diff
Autor:
Weemers, J.J.M., Sypaseuth, F.D., Bäuerlein, P.S., Graaff, van der, W.N.P., Filot, I.A.W., Lutz, M., Mueller, C.
Publikováno v:
European Journal of Organic Chemistry, 2014(2), 350-362. Wiley-VCH Verlag
The development of a novel benzimidazole-derived bidentate P,N-ligand and its application in Ir-catalyzed hydrogenation is described. The ligand backbone was obtained through a one-pot tandem hydroformylation–cyclization sequence and the enantiomer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::fe2a08508100fe009284fb666758825f
https://research.tue.nl/nl/publications/33ba61d8-ec61-490d-8824-5b6abc62f736
https://research.tue.nl/nl/publications/33ba61d8-ec61-490d-8824-5b6abc62f736
Publikováno v:
Proceedings of the Xth Netherlands Catalysis and Chemistry Conference (NCCC XI), 01-03 March 2010, Noordwijkerhout, 194-194
STARTPAGE=194;ENDPAGE=194;TITLE=Proceedings of the Xth Netherlands Catalysis and Chemistry Conference (NCCC XI), 01-03 March 2010, Noordwijkerhout
STARTPAGE=194;ENDPAGE=194;TITLE=Proceedings of the Xth Netherlands Catalysis and Chemistry Conference (NCCC XI), 01-03 March 2010, Noordwijkerhout
only.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::93fa273984361306f27bbf87d0ac4b53
https://research.tue.nl/nl/publications/a52e7d00-c0b2-4363-89af-ed2a0e6e6985
https://research.tue.nl/nl/publications/a52e7d00-c0b2-4363-89af-ed2a0e6e6985
Publikováno v:
Proceedings of the XIth Netherlands Catalysis and Chemistry Conference (NCCC XI), 01-03 March 2010, Noordwijkerhout, 320-320
STARTPAGE=320;ENDPAGE=320;TITLE=Proceedings of the XIth Netherlands Catalysis and Chemistry Conference (NCCC XI), 01-03 March 2010, Noordwijkerhout
STARTPAGE=320;ENDPAGE=320;TITLE=Proceedings of the XIth Netherlands Catalysis and Chemistry Conference (NCCC XI), 01-03 March 2010, Noordwijkerhout
only.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::4b043bf0750201d43670cc565385d7c7
https://research.tue.nl/nl/publications/c66a715b-fe05-48ec-8f5d-6617e3d3959f
https://research.tue.nl/nl/publications/c66a715b-fe05-48ec-8f5d-6617e3d3959f
Publikováno v:
Book of abstracts of the Xth Netherlands Catalysis and Chemistry Conference (NCCC X), 02-04 March 2009, Noordwijkerhout, 310-310
STARTPAGE=310;ENDPAGE=310;TITLE=Book of abstracts of the Xth Netherlands Catalysis and Chemistry Conference (NCCC X), 02-04 March 2009, Noordwijkerhout
STARTPAGE=310;ENDPAGE=310;TITLE=Book of abstracts of the Xth Netherlands Catalysis and Chemistry Conference (NCCC X), 02-04 March 2009, Noordwijkerhout
only.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::0de51f9d324e842f71aafa1cde6f1ef2
https://research.tue.nl/nl/publications/ef9799d9-8bb7-43b9-8e14-ab99101e4a04
https://research.tue.nl/nl/publications/ef9799d9-8bb7-43b9-8e14-ab99101e4a04
Autor:
Bäuerlein, P.S., Arenas Gonzalez, I., Weemers, J.J.M., Lutz, M., Spek, A.L., Vogt, D., Müller, Christian, Rontgen participation programme, Sub Crystal and Structural Chemistry
Publikováno v:
Chemical Communications, 2009(33), 4944. Royal Society of Chemistry
8-Hydroxy-6-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine was formed selectively in high yields from N-(b-methallyl)imidazole by a tandem hydroformylation–cyclization sequence, representing a novel one-pot catalytic synthesis of bicyclic imidazol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::76f5c999ae2e1df2a200c84c31e5fd76
https://dspace.library.uu.nl/handle/1874/43986
https://dspace.library.uu.nl/handle/1874/43986
Autor:
Müller, C., Wasserberg, D., Weemers, J.J.M., Pidko, E.A., Hoffmann, S., Lutz, M., Spek, A.L., Meskers, S.C.J., Jansen, R.A.J., van Santen, R.A., Vogt, D., R¿ntgenparticipatieprogramma, Dep Scheikunde
Publikováno v:
Chemistry-A European Journal, 13(16), 4548. Wiley
A series of donor-functionalized pyrylium salts have been prepared by classical condensation reactions which were further converted into the corresponding thienyl- and pyridyl-substituted polydentate λ3-phosphinines by reaction with P(SiMe3)3. Furth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::e5193f111c92a45752b6475969891685
https://dspace.library.uu.nl/handle/1874/26935
https://dspace.library.uu.nl/handle/1874/26935
Autor:
Weemers, J.J.M., van der Graaff, W.N.P., Pidko, E.A., Lutz, M., Müller, Christian, Crystal and Structural Chemistry, Sub Crystal and Structural Chemistry
Publikováno v:
Chemistry : A European Journal, 19(27), 8991-9004. Wiley-VCH Verlag
Chemistry-A European Journal, 19(27), 8991. Wiley
Chemistry-A European Journal, 19(27), 8991. Wiley
The design and preparation of an asymmetrically substituted and bulky phosphinine was achieved by introducing sterically demanding substituents into specific positions of a rigid phosphorus-heterocyclic framework. Compound 5 shows, at the same time,