Methoxy-substituted centrohexaindanes through the fenestrane route

Tellenbröker, Johannes; Barth, Dieter; Neumann, Beate; Stammler, Hans-Georg; Kuck, Dietmar

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.

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DOI

https://doi.org/10.1039/b471837h

Autor*in

Tellenbröker, Johannes^UniBi; Barth, Dieter^UniBi; Neumann, Beate^UniBi; Stammler, Hans-Georg^UniBi; Kuck, Dietmar^UniBi

Einrichtung

Fakultät für Chemie > Industrielle Organische Chemie und Biotechnologie

Abstract / Bemerkung

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.

Erscheinungsjahr

2005

Zeitschriftentitel

ORGANIC & BIOMOLECULAR CHEMISTRY

Band

Ausgabe

Seite(n)

570-571

ISSN

Page URI

https://pub.uni-bielefeld.de/record/1604923

Zitieren

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. https://doi.org/10.1039/b471837h

Tellenbröker, Johannes, Barth, Dieter, Neumann, Beate, Stammler, Hans-Georg, and Kuck, Dietmar. 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.

Daten bereitgestellt von European Bioinformatics Institute (EBI)

2 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Centrohexaindane: six benzene rings mutually fixed in three dimensions - solid-state structure and six-fold nitration.
Kuck D, Linke J, Teichmann LC, Barth D, Tellenbröker J, Gestmann D, Neumann B, Stammler HG, Bögge H., Phys Chem Chem Phys 18(17), 2016
PMID: 26728545

From Fragmentation to Construction--from Void to Massive: Fascination with Organic Mass Spectrometry and the Synthesis of Novel Three-Dimensional Polycyclic Aromatic Hydrocarbons.
Kuck D., Chem Rec 15(6), 2015
PMID: 26202384

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