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7
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Silverman G.S., and Rakita P.E. (Eds), Marcell Dekker, New York
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In: Silverman G.S., and Rakita P.E. (Eds). Handbook of Grignard Reagents (1996), Marcell Dekker, New York
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Handbook of Grignard Reagents
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8
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4243893500
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For recent reviews on allylations, see:
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For recent reviews on allylations, see:. Yamamoto Y., and Asao N. Chem. Rev. 93 (1993) 2207
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Yamamoto, Y.1
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Bower J.F., Kim I.S., Patman R.L., and Krische M.J. Angew. Chem., Int. Ed. 48 (2009) 34
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Bower, J.F.1
Kim, I.S.2
Patman, R.L.3
Krische, M.J.4
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12
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0142245730
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For reviews on allyl metal carbonyl additions, see:
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For reviews on allyl metal carbonyl additions, see:. Kennedy J.W.J., and Hall D.G. Angew. Chem., Int. Ed. 42 (2003) 4732
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Kennedy, J.W.J.1
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Hill E.A., Boyd W.A., Desai H., Darki A., and Bivens L. J. Organomet. Chem. 514 (1996) 1
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Hill, E.A.1
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36
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Rosales A., Oller-López Juan L., Justica J., Gänsauer A., Oltra J.E., and Cuerva J.M. Chem. Commun. (2004) 2628
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Rosales, A.1
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Cuerva, J.M.6
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37
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62349124157
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Estévez R.E., Justica J., Bazdi B., Fuentes N., Paradas M., Choquesillo-Lazarte D., Garcia-Ruiz J.M., Robles R., Gänsauer A., Cuerva J.M., and Oltra J.E. Chem. Eur. J. 15 (2009) 2774
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Garcia-Ruiz, J.M.7
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Gänsauer, A.9
Cuerva, J.M.10
Oltra, J.E.11
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40
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0030599234
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For the transition metal-catalyzed generation of Grignard reagents, see:
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For the transition metal-catalyzed generation of Grignard reagents, see:. Takai K., Ueda T., Hayashi T., and Moriwake T. Tetrahedron Lett. 37 (1996) 7049
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Takai, K.1
Ueda, T.2
Hayashi, T.3
Moriwake, T.4
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42
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77950021830
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note
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Other phosphines that restore catalytic activity at -40 °C: triphenylphosphine (95%), 1,2-bis(diphenylphosphino)ethane (94%), rac-BINAP (82%), tris(o-tolyl)phosphine (99%), tributylphosphine (95%).
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-
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43
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0030458468
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Allylation of ketones can be problematic, see:
-
Allylation of ketones can be problematic, see:. Fürstner A., and Shi N. J. Am. Chem. Soc. 118 (1996) 12349
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Fürstner, A.1
Shi, N.2
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48
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0027244717
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Ireland R.E., Armstrong J.D., Lebreton J., Meissner R.S., and Rizzacasa M.A. J. Am. Chem. Soc. 115 (1993) 7152
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Ireland, R.E.1
Armstrong, J.D.2
Lebreton, J.3
Meissner, R.S.4
Rizzacasa, M.A.5
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49
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0027244717
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The addition of an allyltitanium complex has been shown to proceed with in a diastereomeric ration of 2:1:
-
The addition of an allyltitanium complex has been shown to proceed with in a diastereomeric ration of 2:1:. Ireland R.E., Armstrong J.D., Lebreton J., Meissner R.S., and Rizzacasa M.A. J. Am. Chem. Soc. 115 (1993) 7152
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(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 7152
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Ireland, R.E.1
Armstrong, J.D.2
Lebreton, J.3
Meissner, R.S.4
Rizzacasa, M.A.5
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