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Results: 67
Number of items: 67
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Delis, J. G. P., Aubel, P. G., van Leeuwen, P. W. N. M., Vrieze, K., Veldman, N., & Spek, A. L. (1995). Isocyanide Insertion into the Palladium-Carbon Bond of (N-N)Pd(Me)Cl Complexes and the Reactivity of the Products toward Norbornadiene; X-ray Structure of (Bipy)Pd(C=N-2,6-MeC2CC6HC4)Me)Cl. Journal of the Chemical Society. Chemical communications, 2233.
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Ruelke, R. E., Delis, J. G. P., Groot, A. M., Elsevier, C. J., van Leeuwen, P. W. N. M., Vrieze, K., Goubitz, K., & Schenk, H. (1995). Insertion Reactions Involving Palladium Complexes with Nitrogen Ligands, Part. I. Reactivity towards Carbon Monoxide of Methylpalladium (II) Complexes containing Bidentate a-Diimine Ligands; X-Ray Structures of Four Methyl- and Acylpalladium (II) Complex. Journal of Organometallic Chemistry. -
de Klerk-Engels, B., Delis, J. G. P., Ernsting, J. M., Elsevier, C. J., Stufkens, D. J., Vrieze, K., Goubitz, K., & Fraanje, J. (1995). Alkene rotation in [CpRu(lC2)(hE2-alkene)][CFC3SOC3] with LE2=iPr- or pTol-diazabutadiene. X-ray structure of [CpRu(pTol-DAB)(hE2-ethene)][CFC3SOC3]. Inorganica Chimica Acta, 273. -
Feiken, N., Frühauf, H.-W., Vrieze, K., Fraanje, J., & Goubitz, K. (1994). 1,3-Dipolar cycloaddition to the Fe-N=C fragment. 14: Aromatic isothiocyanates as dipolarphiles. Reversible formation of novel [3.2.2]bicyclic double isocyanide insertion products. Thermodynamics of isocyanide deinsertion reactions. Organometallics, 13(7), 2285-2832. https://doi.org/10.1021/om00019a044
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van Wijnkoop, M., Ernsting, J. M., Siebenlist, R., de Lange, P. P. M., Fruhauf, H. W., Vrieze, K., Horn, E., & Spek, A. L. (1994). 1,3 Dipolar cycloaddition reactions to the C=X-M fragment. 13. regioselectivity in the reactions of mononuclear iminoketone complexes Fe(CO)sub3(t-Bu=C(H)C(R)=O) with the unsymmetrical alkyne methyl propynoate. Journal of Organometallic Chemistry, 482, 99-109. https://doi.org/10.1016/0022-328X(94)88190-1
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Feiken, N., Fruhauf, H. W., & Vrieze, K. (1994). 1,3 Dipolar cycloaddition to the Fe-N=C fragment. 14. Aromatic isothiocyanates as dipolarophiles. Reversible formation of novel [3.2.2] bicyclic double isocyanide deinsertion reactions. Organometallics, 13, 2825-2832. https://doi.org/10.1021/om00019a044
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