Methoxy-substituted centrohexaindanes through the fenestrane route

Tellenbröker J, Barth D, Neumann B, Stammler H-G, Kuck D (2005)
ORGANIC & BIOMOLECULAR CHEMISTRY 3(4): 570-571.

Journal Article | Published | English

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Abstract
Tetrahydroxyfenestrindane undergoes HPF6-catalyzed condensation with anisole, 2- methylanisole and the three dimethoxybenzenes to furnish several centrohexaindanes bearing oxyfunctionalization at the opposite ends of one of the three [2,2]- spirobiindane axes.
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Tellenbröker J, Barth D, Neumann B, Stammler H-G, Kuck D. Methoxy-substituted centrohexaindanes through the fenestrane route. ORGANIC & BIOMOLECULAR CHEMISTRY. 2005;3(4):570-571.
Tellenbröker, J., Barth, D., Neumann, B., Stammler, H. - G., & Kuck, D. (2005). Methoxy-substituted centrohexaindanes through the fenestrane route. ORGANIC & BIOMOLECULAR CHEMISTRY, 3(4), 570-571.
Tellenbröker, J., Barth, D., Neumann, B., Stammler, H. - G., and Kuck, D. (2005). Methoxy-substituted centrohexaindanes through the fenestrane route. ORGANIC & BIOMOLECULAR CHEMISTRY 3, 570-571.
Tellenbröker, J., et al., 2005. Methoxy-substituted centrohexaindanes through the fenestrane route. ORGANIC & BIOMOLECULAR CHEMISTRY, 3(4), p 570-571.
J. Tellenbröker, et al., “Methoxy-substituted centrohexaindanes through the fenestrane route”, ORGANIC & BIOMOLECULAR CHEMISTRY, vol. 3, 2005, pp. 570-571.
Tellenbröker, J., Barth, D., Neumann, B., Stammler, H.-G., Kuck, D.: Methoxy-substituted centrohexaindanes through the fenestrane route. ORGANIC & BIOMOLECULAR CHEMISTRY. 3, 570-571 (2005).
Tellenbröker, Johannes, Barth, Dieter, Neumann, Beate, Stammler, Hans-Georg, and Kuck, Dietmar. “Methoxy-substituted centrohexaindanes through the fenestrane route”. ORGANIC & BIOMOLECULAR CHEMISTRY 3.4 (2005): 570-571.
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