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1
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57649224066
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I-H:, - 11528
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I-H:, S. Rendler, O. Plefka, B. Karatas, G. Auer, R. Fröhlich, C. Mück-Lichtenfeld, S. Grimme, M. Oestreich, Chem. Eur. J. 2008, 14, 11512 - 11528
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52649092372
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I-B:, - 4454
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I-B:, L. Dang, Z. Lin, T. B. Marder, Organometallics 2008, 27, 4443 - 4454
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Dang, L.1
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3
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78149426752
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I-Si: we are not aware of any reports related to the mechanism of this transmetalation
-
I-Si: we are not aware of any reports related to the mechanism of this transmetalation.
-
-
-
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4
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51049123834
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2927
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I-H in conjugate addition, see C. Deutsch, N. Krause, B. H. Lipshutz, Chem. Rev. 2008, 108, 2916 - 2927
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Deutsch, C.1
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7
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1216
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I-B in conjugate addition, see J. A. Schiffner, K. Müther, M. Oestreich, Angew. Chem. 2010, 122, 1214 - 1216
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Schiffner, J.A.1
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Angew. Chem. Int. Ed. 2010, 49, 1194 - 1196
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(2010)
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10
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77949410450
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I-Si in conjugate addition, see, - 2900
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I-Si in conjugate addition, see, K.-s. Lee, A. H. Hoveyda, J. Am. Chem. Soc. 2010, 132, 2898 - 2900.
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L. K, -S.1
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70349682627
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5852
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I-H in propargylic substitution, see C. Zhong, Y. Sasaki, H. Ito, M. Sawamura, Chem. Commun. 2009, 5850 - 5852
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(2009)
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Zhong, C.1
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5012
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C. Deutsch, N. Krause, B. H. Lipshutz, Org. Lett. 2009, 11, 5010 - 5012.
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Deutsch, C.1
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13
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28044443673
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16035
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I-B in allylic substitution, see H. Ito, C. Kawakami, M. Sawamura, J. Am. Chem. Soc. 2005, 127, 16034 - 16035
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(2005)
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18
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78149457443
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I-Si in allylic substitution by transmetalation of interelement bonds. This is the topic of the present investigation
-
I-Si in allylic substitution by transmetalation of interelement bonds. This is the topic of the present investigation.
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20
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5644244497
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2142; allylic substitution
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M. Oestreich, B. Weiner, Synlett 2004, 2139 - 2142; allylic substitution
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(2004)
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M. Oestreich, G. Auer, Adv. Synth. Catal. 2005, 347, 637 - 640; alkyne, diene, and styrene addition
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Oestreich, M.1
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570, and references therein
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Vyas, D.J.1
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25
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78149447785
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2PhSiBpin activation are
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2PhSiBpin activation are Ref.-[4]
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26
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77954545005
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4847
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M. Tobisu, H. Fujihara, K. Koh, N. Chatani, J. Org. Chem. 2010, 75, 4841 - 4847.
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30
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78149449588
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[17] We, therefore, decided to study the related copper(I) catalysis
-
[17] We, therefore, decided to study the related copper(I) catalysis.
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31
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53249128754
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3820
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6198
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78149441912
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K. Müther, M. Oestreich, unpublished results, 2009
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K. Müther, M. Oestreich, unpublished results, 2009.
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40
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33750350817
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2PhSiBpin, see, - 13683
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2PhSiBpin, see, T. Ohmura, H. Taniguchi, M. Suginome, J. Am. Chem. Soc. 2006, 128, 13682 - 13683.
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78149438407
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For a review of the chemistry of allylic silanes, see
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For a review of the chemistry of allylic silanes, see
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42
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3199; for the preparation of allylic silanes, see
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L. Chabaud, P. James, Y. Landais, Eur. J. Org. Chem. 2004, 3173 - 3199; for the preparation of allylic silanes, see
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43
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in (Ed.: I. Fleming), Thieme, Stuttgart
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Sarkar, T.K.1
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44
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77955124931
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3347
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For recent (indirect syntheses) of α-chiral allylic silane, see D. Li, T. Tanaka, H. Ohmiya, M. Sawamura, Org. Lett. 2010, 12, 3344 - 3347
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47
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78149453342
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-
note
-
A few test runs using binap (rs=98:2) and josiphos (rs=90:10) yielded only racemic γ- 2 a, not even reaching full conversion after several days at ambient temperature (binap=2,2′-bis(diphenylphosphanyl)-1,1′- binaphthyl and josiphos=1-[2-(diphenylphosphanyl)ferrocenyl] ethyldicyclohexylphosphine).
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