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0003024555
-
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-1 at -33 °C. Assuming that 1 has a similar energy barrier, we calculated the half-life for racemization to be shorter than 0.004 s: Fabbri, D.; Dore, A.; Gladiali, S.; De Lucchi, O.; Valle, G. Gazz. Chim. Ital. 1996, 126, 11.
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25
-
-
0011152270
-
-
note
-
2 can be used as well, although the reaction rate is a little slower.
-
-
-
-
26
-
-
0011145735
-
-
note
-
THF is a solvent of choice because the dinaphthothiophene 1 is not soluble in other solvents (benzene, toluene, or diethyl ether) usually used for the Grignard cross-coupling.
-
-
-
-
27
-
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0001254371
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Hayashi, T.; Han, J.-W.; Takeda, A.; Tang, J.; Nohmi, K.; Mukaide, K.; Tsuji, H.; Uozumi, Y. Adv. Synth. Catal. 2001, 343, 279.
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28
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0000259867
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Tamao, K.; Sumitani, K.; Kiso, Y.; Zembayashi, M.; Fujioka, A.; Kodama, S.; Nakajima, I.; Minato, A.; Kumada, M. Bull. Chem. Soc. Jpn. 1976, 49, 1958.
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Kumada, M.9
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29
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0033603883
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The oxidative addition of a dibenzothiophene to a nickel species forming a nickelacycle complex has been reported: Vicic, D. A.; Jones, W. D. J. Am. Chem. Soc. 1999, 121, 7606.
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Vicic, D.A.1
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-
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0011118282
-
-
note
-
D +145 (c 1.0, chloroform)) of the authentic sample prepared from -binaphthol (ref 12).
-
-
-
-
31
-
-
0039599114
-
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Hoffmann, R. W.; Hölzer, B.; Knopff, O.; Harms, K. Angew, Chem., Int. Ed. 2000, 39, 3072.
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Hoffmann, R.W.1
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32
-
-
0011154845
-
-
note
-
The MOP ligand 15 is useful as a chiral ligand for the palladium-catalyzed asymmetric hydrosilylation of 1,3-dienes (ref 12).
-
-
-
-
33
-
-
0032917881
-
-
Similar asymmetric ring-opening reactions of biaryl lactones have been studied extensively by Bringmann: Bringmann, G.; Breuning, M.; Tasler, S. Synthesis 1999, 525.
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Bringmann, G.1
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