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Online, John Wiley & Sons Ltd, in press, DOI: 10.1002/047084289X.rn00968
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Encyclopedia of Reagents for Organic Synthesis
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3 base was used, while FC-1029 gave 100% conversion (entry 4) under identical conditions.
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3 base was used, while FC-1029 gave 100% conversion (entry 4) under identical conditions.
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Parrish, C. A.; Buchwald, S. L. J. Am. Chem. Soc. 2001, 66, 3820-27. See also references for supported catalysts in aryl iodide and bromide coupling.
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Parrish, C. A.; Buchwald, S. L. J. Am. Chem. Soc. 2001, 66, 3820-27. See also references for supported catalysts in aryl iodide and bromide coupling.
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Currently we have full elemental analyses for these complexes of FC-1029 series (see Supporting Information, Preliminary solid state 31P NMR data of the FibreCat samples were obtained with the help of Prof. Mark Smith, Warwick University. FibreCat-1029 was used as a standard. FibreCat-1029 gave a single broad peak at 30-35 ppm, with associated spinning side-bands. This is assigned to be polymer-bound-PPh2 complexed to Pd(II, For FibreCat-1032 the main peak for-PPh2 is shifted to ca. 20 ppm (presumably due to trans effect of the PtBu3 ligand displacing MeCN) in addition to a new peak at ca. 40 ppm. The area for the second peak is smaller than that Of-PPh2, suggesting incomplete substitution with the bulky t-Bu3P ligand. As expected, where the added ligand contains only aryl substituents, as is the case for BINAP FibreCat-1036, separate resonances are not resolved. For FibreCat-1039, containing the polymer-b
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2 groups remain unreacted with Pd. The presence of these additional sites further complicates the spectral interpretation for FibreCat-1045 and -1046. Therefore detailed solid state NMR and surface characterization studies are required.
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