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more..
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6
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33847630844
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note
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++1).
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7
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0001726105
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Izatt R.M., Nelson D.P., Rytting J.H., Haymore B.L., and Christensen J.J. J. Am. Chem. Soc. 93 (1971) 1619-1623
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Haymore, B.L.4
Christensen, J.J.5
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9
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0000358709
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The preparation of the non commercial benzylzinc reagents was conducted applying the conditions developed by Rieke from benzylic bromides and chlorides:
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The preparation of the non commercial benzylzinc reagents was conducted applying the conditions developed by Rieke from benzylic bromides and chlorides:. Zhu L., Wehmeyer R.M., and Rieke R.D. J. Org. Chem. 56 (1991) 1445-1453
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Zhu, L.1
Wehmeyer, R.M.2
Rieke, R.D.3
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10
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0000290760
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The cross coupling was conducted using standard conditions related to aryl halides:
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The cross coupling was conducted using standard conditions related to aryl halides:. Minato A., Tamao K., Hayashi T., Suzuki K., and Kumada M. Tetrahedron Lett. 21 (1980) 845-848
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Minato, A.1
Tamao, K.2
Hayashi, T.3
Suzuki, K.4
Kumada, M.5
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12
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33847639348
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note
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With this substituent, the reaction time was only 20 min in order to avoid formation of side overcoupling material.
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