Synthesis of 2,3,6,7-tetrabromoanthracene
Schäfer C, Herrmann F, Mattay J (2008)
Beilstein Journal of Organic Chemistry (4): 41.
Zeitschriftenaufsatz
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Autor*in
Schäfer, Christian;
Herrmann, FriederikeUniBi;
Mattay, JochenUniBi
Einrichtung
Abstract / Bemerkung
The first synthesis of 2,3,6,7-tetrabromoanthracene is presented, starting from benzene in a straightforward four step synthesis.
Stichworte
7-tetrabromoanthracene;
arenes;
anthracene;
cyclizations;
polycycles;
2;
ring closure;
6;
3
Erscheinungsjahr
2008
Zeitschriftentitel
Beilstein Journal of Organic Chemistry
Ausgabe
4
Art.-Nr.
41
ISSN
1860-5397
Page URI
https://pub.uni-bielefeld.de/record/1636597
Zitieren
Schäfer C, Herrmann F, Mattay J. Synthesis of 2,3,6,7-tetrabromoanthracene. Beilstein Journal of Organic Chemistry. 2008;(4): 41.
Schäfer, C., Herrmann, F., & Mattay, J. (2008). Synthesis of 2,3,6,7-tetrabromoanthracene. Beilstein Journal of Organic Chemistry(4), 41. https://doi.org/10.3762/bjoc.4.41
Schäfer, Christian, Herrmann, Friederike, and Mattay, Jochen. 2008. “Synthesis of 2,3,6,7-tetrabromoanthracene”. Beilstein Journal of Organic Chemistry, no. 4: 41.
Schäfer, C., Herrmann, F., and Mattay, J. (2008). Synthesis of 2,3,6,7-tetrabromoanthracene. Beilstein Journal of Organic Chemistry:41.
Schäfer, C., Herrmann, F., & Mattay, J., 2008. Synthesis of 2,3,6,7-tetrabromoanthracene. Beilstein Journal of Organic Chemistry, (4): 41.
C. Schäfer, F. Herrmann, and J. Mattay, “Synthesis of 2,3,6,7-tetrabromoanthracene”, Beilstein Journal of Organic Chemistry, 2008, : 41.
Schäfer, C., Herrmann, F., Mattay, J.: Synthesis of 2,3,6,7-tetrabromoanthracene. Beilstein Journal of Organic Chemistry. : 41 (2008).
Schäfer, Christian, Herrmann, Friederike, and Mattay, Jochen. “Synthesis of 2,3,6,7-tetrabromoanthracene”. Beilstein Journal of Organic Chemistry 4 (2008): 41.
1 Zitation in Europe PMC
Daten bereitgestellt von Europe PubMed Central.
(Hetero)aromatics from dienynes, enediynes and enyne-allenes.
Raviola C, Protti S, Ravelli D, Fagnoni M., Chem Soc Rev 45(15), 2016
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Raviola C, Protti S, Ravelli D, Fagnoni M., Chem Soc Rev 45(15), 2016
PMID: 27263976
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