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A non-photochemical route to synthesize simple benzo[1,2-b:4,3-b′] dithiophenes: FeCl3-mediated cyclization of dithienyl ethenes

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A non-photochemical route to synthesize simple benzo[1,2-b:4,3-b′] dithiophenes: FeCl3-mediated cyclization of dithienyl ethenes. / Cauteruccio, Silvia; Dova, Davide; Graiff, Claudia et al.
In: New Journal of Chemistry, Vol. 38, No. 6, 30.06.2014, p. 2241-2244.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Cauteruccio, S, Dova, D, Graiff, C, Carrara, C, Doulcet, J, Stephenson, GR & Licandro, E 2014, 'A non-photochemical route to synthesize simple benzo[1,2-b:4,3-b′] dithiophenes: FeCl3-mediated cyclization of dithienyl ethenes', New Journal of Chemistry, vol. 38, no. 6, pp. 2241-2244. https://doi.org/10.1039/c3nj01567j

APA

Cauteruccio, S., Dova, D., Graiff, C., Carrara, C., Doulcet, J., Stephenson, G. R., & Licandro, E. (2014). A non-photochemical route to synthesize simple benzo[1,2-b:4,3-b′] dithiophenes: FeCl3-mediated cyclization of dithienyl ethenes. New Journal of Chemistry, 38(6), 2241-2244. https://doi.org/10.1039/c3nj01567j

Vancouver

Cauteruccio S, Dova D, Graiff C, Carrara C, Doulcet J, Stephenson GR et al. A non-photochemical route to synthesize simple benzo[1,2-b:4,3-b′] dithiophenes: FeCl3-mediated cyclization of dithienyl ethenes. New Journal of Chemistry. 2014 Jun 30;38(6):2241-2244. doi: 10.1039/c3nj01567j

Author

Cauteruccio, Silvia ; Dova, Davide ; Graiff, Claudia et al. / A non-photochemical route to synthesize simple benzo[1,2-b:4,3-b′] dithiophenes : FeCl3-mediated cyclization of dithienyl ethenes. In: New Journal of Chemistry. 2014 ; Vol. 38, No. 6. pp. 2241-2244.

Bibtex

@article{d08a007795104232ac12e2e2b5515d4c,
title = "A non-photochemical route to synthesize simple benzo[1,2-b:4,3-b′] dithiophenes: FeCl3-mediated cyclization of dithienyl ethenes",
abstract = "The FeCl3-mediated cyclization of α,α′- disubstituted Z-alkenes 1 is reported as a general and non-photochemical route to synthesize benzo[1,2-b:4,3-b′]dithiophene (BDT) derivatives 2, achievable in good yields starting from cheap and easily available materials. The influence of the temperature and the nature of the substituents on the scope and limitations of this methodology is also reported. This journal is",
author = "Silvia Cauteruccio and Davide Dova and Claudia Graiff and Claudio Carrara and Julien Doulcet and Stephenson, {G. Richard} and Emanuela Licandro",
year = "2014",
month = jun,
day = "30",
doi = "10.1039/c3nj01567j",
language = "English",
volume = "38",
pages = "2241--2244",
journal = "New Journal of Chemistry",
issn = "1144-0546",
publisher = "Royal Society of Chemistry",
number = "6",

}

RIS

TY - JOUR

T1 - A non-photochemical route to synthesize simple benzo[1,2-b:4,3-b′] dithiophenes

T2 - FeCl3-mediated cyclization of dithienyl ethenes

AU - Cauteruccio, Silvia

AU - Dova, Davide

AU - Graiff, Claudia

AU - Carrara, Claudio

AU - Doulcet, Julien

AU - Stephenson, G. Richard

AU - Licandro, Emanuela

PY - 2014/6/30

Y1 - 2014/6/30

N2 - The FeCl3-mediated cyclization of α,α′- disubstituted Z-alkenes 1 is reported as a general and non-photochemical route to synthesize benzo[1,2-b:4,3-b′]dithiophene (BDT) derivatives 2, achievable in good yields starting from cheap and easily available materials. The influence of the temperature and the nature of the substituents on the scope and limitations of this methodology is also reported. This journal is

AB - The FeCl3-mediated cyclization of α,α′- disubstituted Z-alkenes 1 is reported as a general and non-photochemical route to synthesize benzo[1,2-b:4,3-b′]dithiophene (BDT) derivatives 2, achievable in good yields starting from cheap and easily available materials. The influence of the temperature and the nature of the substituents on the scope and limitations of this methodology is also reported. This journal is

U2 - 10.1039/c3nj01567j

DO - 10.1039/c3nj01567j

M3 - Journal article

AN - SCOPUS:84901023895

VL - 38

SP - 2241

EP - 2244

JO - New Journal of Chemistry

JF - New Journal of Chemistry

SN - 1144-0546

IS - 6

ER -