Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jos Wilting"'
Publikováno v:
Angewandte Chemie-International Edition, 49(42), 7738-7741. Wiley
Angewandte Chemie, 122(42), 7904-7907. Wiley-VCH Verlag
Angewandte Chemie, 122(42), 7904-7907. Wiley-VCH Verlag
Go with the flow: Homogeneous catalyst recycling can be applied to the production of aldehydes in a continuous flow nanofiltration reactor (see picture) that can operate for an unprecedented period of up to two weeks without showing typical deactivat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f1ecc7a94924d9440db0c9b6aefac22
https://research.tue.nl/en/publications/1a6501fc-ab1a-45fc-b237-060df91103fe
https://research.tue.nl/en/publications/1a6501fc-ab1a-45fc-b237-060df91103fe
Autor:
Christian Müller, Anthony L. Spek, Dieter Vogt, Mcc Michèle Janssen, Jbm Jos Wilting, Martin Lutz
Publikováno v:
Wilting, J, Janssen, M H M, Muller, C J, Lutz, M, Spek, A L & Vogt, D 2007, ' Binaphthol-based diphosphite ligands in asymmetric nickel-catalyzed hydrocyanation of styrene and 1,3-cyclohexadiene: Influence of steric properties ', Advanced Synthesis and Catalysis, vol. 349, no. 3, pp. 350-356 . https://doi.org/10.1002/adsc.200600315
Advanced Synthesis & Catalysis, 349(3), 350-356. Wiley-VCH Verlag
Advanced Synthesis and Catalysis, 349(3), 350-356. Wiley-VCH Verlag
Advanced Synthesis & Catalysis, 349(3), 350-356. Wiley-VCH Verlag
Advanced Synthesis and Catalysis, 349(3), 350-356. Wiley-VCH Verlag
A series of chiral (R)-binaphthol-based di- phosphite ligands with different substituents was pre- pared and applied in the asymmetric nickel-catalyzed hydrocyanation of styrene and 1,3-cyclohexadiene to investigate the influence of their steric prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0b25f980eb1e2a04bd43b211d7f7a90
https://hdl.handle.net/1871/30952
https://hdl.handle.net/1871/30952
Autor:
Jos Wilting, Dieter Vogt
The asymmetric hydrocyanation of olefins is an atom efficient carbon–carbon bond forming reaction, in which nitriles are produced that can be converted into a variety of products. Examples of asymmetric hydrocyanation of norbornene, vinylarenes and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85a5ea38ca8748b15d15e42b971d1250
https://doi.org/10.1016/b978-0-08-095167-6.00517-6
https://doi.org/10.1016/b978-0-08-095167-6.00517-6
Autor:
Dieter Vogt, Jbm Jos Wilting
Publikováno v:
Handbook of C–H Transformations
The whole range of the functionalization of CH-bonds presented for the first time in two volumes. The focus throughout is on topicality and practicability, with reliable and typical experimental procedures included.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::805468c8c67d86b48dd13d058f9f9bb0
https://doi.org/10.1002/9783527619450.ch4
https://doi.org/10.1002/9783527619450.ch4
Autor:
Lars von Chrzanowski, Christian Müller, and Anthony L. Spek, Dieter Vogt, Jos Wilting, Laura Bini
Publikováno v:
Journal of the American Chemical Society, 129(42), 12622-12623. American Chemical Society
A triptycene-based diphosphine ligand was synthesized in good yield following a new route. The corresponding Pt(II)- and Ni(0)-complexes were characterized. In butadiene hydrocyanation the tript-PPh2Ni(cod) catalyst leads to exceptionally high select
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f48d2d5ac3a35681e63a3fdd98194eb
https://dspace.library.uu.nl/handle/1874/26892
https://dspace.library.uu.nl/handle/1874/26892
Autor:
Jos Wilting, Dianne D. Ellis, Alison Hewat, Dieter Vogt, and Anthony L. Spek, Christian Müller, Duncan M. Tooke
Publikováno v:
Organometallics, 24(1), 13-15. American Chemical Society
The isomerization of the branched 2M3BN to the linear 3PN by a DPEphosNi species has been investigated by means of variable-temperature NMR spectroscopy, and activation parameters have been determined. An intermediate in this reaction, which is forme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1c4a95e9dd1b16c2af280b3f5872f9c
https://research.tue.nl/nl/publications/000d0c1c-57d8-4aca-bc61-e6e6d83d8fbf
https://research.tue.nl/nl/publications/000d0c1c-57d8-4aca-bc61-e6e6d83d8fbf
Publikováno v:
Wilting, J, Janssen, M H M, Muller, C J & Vogt, D 2006, ' The enantioselective step in the nickel-catalyzed hydrocyanation of 1,3-cyclohexadiene ', Journal of the American Chemical Society, vol. 128, no. 35, pp. 11374-5 . https://doi.org/10.1021/ja064378u
Journal of the American Chemical Society, 128(35), 11374-11375. American Chemical Society
Journal of the American Chemical Society, 128(35), 11374-5. American Chemical Society
Journal of the American Chemical Society, 128(35), 11374-11375. American Chemical Society
Journal of the American Chemical Society, 128(35), 11374-5. American Chemical Society
On the basis of deuterium labeling experiments and an equal 1,2-/1,4-product distribution, the reductive elimination of the product has been established to be the enantioselective step in the nickel-catalyzed hydrocyanation of 1,3-cyclohexadiene. Thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edca6a89b032a47abdde7f50bf5e60e9
https://hdl.handle.net/1871/27870
https://hdl.handle.net/1871/27870
Publikováno v:
Acta Crystallographica, Section E: Structure Reports, E61(8), o2406-o2407. International Union of Crystallography
The title compound, C36H28O2P2, features weak inter- and intramolecular hydrogen bonds linking molecules into infinite chains.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a74e16b4ab5f0368458f633581d7870e
https://doi.org/10.1107/S1600536805020805
https://doi.org/10.1107/S1600536805020805
Publikováno v:
Angewandte Chemie; Oct2010, Vol. 122 Issue 42, p7904-7907, 4p