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14
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26844459481
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Obtained from Fluka, 1.7 mmol/g Cl, 1% crosslinked
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Obtained from Fluka, 1.7 mmol/g Cl, 1% crosslinked.
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15
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26844562850
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Patent, US 5,324,483,1994
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For previous examples of ketalization of diols with ketones on the solid phase see: a) D. M. Reynolds Cody, S. H, Hobbs DeWitt, J. C. Hodges, J. S. Kiely, W. M. Moos, M. R. Pavia, B. D. Roth, M. C. Schroeder, C. J. Stankovic, Patent, US 5,324,483,1994.
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18
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0002479605
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d) S. Hanessian, T. Ogawa, Y. Guindon, J. L. Kamennof, R. Roy, Carbohydrate Research 1974, 38, C15-C18.
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Roy, R.5
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19
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26844453284
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note
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Elemental analysis for chlorine or bromine suggested a loading of 0.5-0.7 mmol/g, a yield of 41-57% based on the loading of the commercial Merrifield resin.
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20
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0029049463
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a) J. Y. Roberge, X. Beebe, S. J. Danishefsky, Science 1995, 269, 202-204.
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0027591808
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b) S. J. Danishefsky, K. F. McClure, J. T. Randolph, R. B. Ruggeri, Science 1993, 260, 1307-1309.
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22
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26844437602
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note
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In some examples, Pd(0)-coupling was performed prior to the acylation step, with equally good results.
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23
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85005759612
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T. Hudlicky, F. Rulin, T. Tsunoda, H. Luna, C. Andersen, J. D. Price Isr. J. Chem. 1991, 31, 229-238. In the examples studied, facial selectivity is not influenced by the solid phase: facial selectivity was identical when reactions were performed in solution with acetonide protected substrates.
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Hudlicky, T.1
Rulin, F.2
Tsunoda, T.3
Luna, H.4
Andersen, C.5
Price, J.D.6
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