Preparation and Characterization of 3,4-Diaryl-Substituted 2-Diarylamino­thiophenes

Olaf Zeika; Horst Hartmann

doi:10.1055/s-2004-815933

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Synthesis 2004(3): 377-380
DOI: 10.1055/s-2004-815933

PAPER

Preparation and Characterization of 3,4-Diaryl-Substituted 2-Diarylaminothiophenes

Olaf Zeika^a, Horst Hartmann*^b
^a Institute of Applied Photophysics, Technical University Dresden, Mommsenstr. 13, 01346 Dresden, Germany
^b Department of Chemistry, University of Applied Sciences, Geusaer Str., 06217 Merseburg, Germany
Fax: +49(3461)462192; e-Mail: Horst.Hartmann@cui.fh-merseburg.de;

Further Information

Publication History

Received 24 October 2003
Publication Date:
26 January 2004 (online)

Abstract
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Abstract

Starting from N,N,C-triarylacetamides and 1-aryl-2-bromoethanones a series of new 3,4-diaryl-substituted 2-diarylaminothiophenes have been prepared and characterized spectroscopically.

Key words

amines - cyclization - heterocycles - oxidations

References

1a Bedworth PV. Marder SR. Jen AK.-Y. Cai M. J. Org. Chem. 1996, 61: 2242

Crossref Google Scholar
1b Jen AK.-Y. Cai Y. Bedworth PV. Marder SR. Adv. Mater. 1997, 9: 132

Crossref Google Scholar
1c Shoshi MNS. inventors; Sasaki M. S. S. DE 3 439 113. ; Chem. Abstr. 1986, 104: 59361

Crossref
2a Gerstner P. Rohde D. Hartmann H. Synthesis 2002, 2487

Crossref Google Scholar
2b Wong KT. Hung TH. Kao SC. Chou CH. Su YO. Chem. Commun. 2001, 1628

Crossref Google Scholar
3a Goodbrand HC. Hu NX. J. Org. Chem. 1999, 64: 670

Google Scholar
3b O’Brien DF. Burrows PE. Forrest SR. Koene BE. Loy DE. Thompson ME. Adv. Mater. 1998, 10: 1109

Google Scholar
4 Shirota Y. J. Mater. Chem. 2000, 10: 1

Crossref Google Scholar
5 Fuhrmann T. Salbeck J. Adv. Photochem. 2002, 27: 83

Google Scholar
6 Getautis V. Stanisauskaite A. Paululis O. Uss S. Uss V. J. Prakt. Chem. 2000, 342: 58

Crossref Google Scholar
7a Johnson GE. McGrane KM. Stolka M. Pure Appl. Chem. 1995, 67: 175

Crossref Google Scholar
7b Noda T. Ogawa H. Noma N. Shirota Y. J. Mater. Chem. 1999, 9: 2177

Crossref Google Scholar
7c Shirota Y. Okumoto K. Inada H. Synth. Met. 2000, 111-112: 387

Crossref Google Scholar
8 Horowitz G. Adv. Mater. 1998, 10: 365

Crossref Google Scholar
9a Cariciftci NS. Smilowitz L. Heeger AJ. Wudl F. Science 1992, 258: 1474

Google Scholar
9b Halls JJM. Walsh CA. Greenham NC. Marseglia EA. Friend RH. Moratti SC. Holmes AB. Nature (London, U.K.) 1965, 376: 498

Google Scholar
10 Tabet A. Schröder A. Hartmann H. Rohde D. Dunsch L. Org. Lett. 2003, 5: 1817

Crossref Google Scholar
11a Effenberger F. Würthner F. Steybe F. J. Org. Chem. 1995, 60: 2082

Crossref Google Scholar
11b Noack A. Hartmann H. Chem. Lett. 2002, 644

Crossref Google Scholar
12a Kisselev R. Thelakkat M. Chem. Commun. 2002, 1530

Crossref Google Scholar
12b Wu IY. Lin JT. Tao Y.-T. Balasubramaniam E. Su YZ. Ko C.-W. Chem. Mater. 2001, 13: 2626

Crossref Google Scholar
13 Hartmann H. Gerstner P. Rohde D. Org. Lett. 2001, 3: 1673

Crossref Google Scholar
14a McCullough RD. Adv. Mater. 1998, 10: 93

Crossref Google Scholar
14b Roncali J. Chem. Rev. 1992, 92: 711

Crossref Google Scholar
15 Hartmann H. Mayer R. Z. Chem. 1966, 6: 28

Google Scholar
16 Schumann J. Kanitz A. Hartmann H. Synthesis 2002, 1268

Article in Thieme Connect Google Scholar
18 Hammerich O. Parker VD. Adv. Phys. Org. Chem. 1984, 20: 55

Google Scholar

17

Zeika, O.; Hartmann, H. European Patent claimed.