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Cyclohexyl phenylmethanol

Diphenylzinc (0.32 mmol) is added to a Schlenk flask kept in a dry box. The flask is removed from the dry box and fresh hexane (6 ml) is added, followed by EtjZn (1 M in hexane, 0.66 mmol) [75]. The reaction mixture is stirred [Pg.372]

A Pmtical Approach, 2nd Thoroughly Revised and Updated edn, Wiley-VCH Verlag GmbH, Weinheim. [Pg.373]

Ackermann, L. (2009) Modern Arylation Meth- 49. ods, Wiley-VCH Verlag GmbH Co. KGaA, Weinheim. [Pg.374]

Hiyama, T. (2000) Organofluorine Compounds. 53. Chemistry and Applications, Springer, New York. Martina, S.L.X., Jagt, R.B.C., Vries, J.G.d., [Pg.374]

Suzuki, K., Arao, T, Ishii, S., Maeda, Y, Kondo, 61. K., and Aoyama, T. (2006) Tetrahedron Lett, 47, [Pg.374]


See other pages where Cyclohexyl phenylmethanol is mentioned: [Pg.372]    [Pg.372]   


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