144
C. D. Roy and H. C. Brown
bromohydrins were extracted with CH2Cl2 (3 × 35 mL), and the
combined organic layers dried (anhydrous MgSO4) and concen-
trated in vacuum. The percentage chemical transformation of
bromohydrins and the recovered reactive compounds were deter-
mined by 1H NMR spectroscopy using biphenyl (0.25 mmol) as
an internal standard.
(b) H. Sharghi, A. R. Massah, H. Eshghi, K. Niknam, J. Org. Chem.
1998, 63, 1455. doi:10.1021/JO971453Y
(c) H. Kotsuki,T. Shimanouchi, R. Ohshima, S. Fujiwara,Tetrahedron
1998, 54, 2709. doi:10.1016/S0040-4020(98)83007-X
(d)G. Sabitha, R. S. Babu, M. Rajkumar, C. S. Reddy, J. S.Yadav,Tetra-
hedron Lett. 2001, 42, 3955. doi:10.1016/S0040-4039(01)00622-0
(e) M.A. Reddy, K. Surendra, N. Bhanumathi, K. R. Rao,Tetrahedron
2002, 58, 6003. doi:10.1016/S0040-4020(02)00614-2
(f) J. M. Bartas-Yacoubou, N. Maduike, S. Kyere, L. Doan,
D. L. Whalen, Tetrahedron Lett. 2002, 43, 3781. doi:10.1016/S0040-
4039(02)00637-8
Acknowledgments
Financial supports from the Purdue Borane Research Fund and the Herbert
C. Brown Center for Borane Research are gratefully acknowledged.
(g) K. Niknam, T. Nasehi, Tetrahedron 2002, 58, 10259.
doi:10.1016/S0040-4020(02)01349-2
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