Abstract
A series of substituted alkoxy compounds of titanium were prepared by reactions of titanium isopropylate with 1-menthol, 1-borneol, (±)-isoborneol, and (-)-trans-3-hydroxymyrtanol. The specific rotation of the alcoholates was shown to be an additive function of the number of the terpene ligands. For titanium bornylates, the optical activity is a linear function of the degree of substitution. For trans-3-hydroxymyrtanol derivatives, an inversion of the optical rotation angle is observed along with an additive dependence of the optical activity on the degree of substitution.
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Original Russian Text © Yu.S. Matveev, L.L. Frolova, N.A. Kataeva, A.V. Kuchin, 2007, published in Zhurnal Obshchei Khimii, 2007, Vol. 77, No. 7, pp. 1112–1119.
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Matveev, Y.S., Frolova, L.L., Kataeva, N.A. et al. Chiral derivatives of titanium with terpene alcohols. Russ J Gen Chem 77, 1196–1203 (2007). https://doi.org/10.1134/S1070363207070109
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DOI: https://doi.org/10.1134/S1070363207070109