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Synthesis of dithienoquinazolines from pyrimidines via intramolecular nucleophilic aromatic substitution of hydrogen. / Verbitskiy, Egor V.; Dinastiya, Ekaterina M.; Baranova, Anna A.; Eltsov, Oleg S.; Rusinov, Gennady L.; Chupakhin, Oleg N.; Charushin, Valery N.

In: Chemistry of Heterocyclic Compounds, Vol. 53, No. 10, 01.10.2017, p. 1156-1160.

Research output: Contribution to journal › Article › peer-review

Harvard

Verbitskiy, EV, Dinastiya, EM, Baranova, AA, Eltsov, OS, Rusinov, GL, Chupakhin, ON & Charushin, VN 2017, 'Synthesis of dithienoquinazolines from pyrimidines via intramolecular nucleophilic aromatic substitution of hydrogen', Chemistry of Heterocyclic Compounds, vol. 53, no. 10, pp. 1156-1160. https://doi.org/10.1007/s10593-017-2188-4

APA

Verbitskiy, E. V., Dinastiya, E. M., Baranova, A. A., Eltsov, O. S., Rusinov, G. L., Chupakhin, O. N., & Charushin, V. N. (2017). Synthesis of dithienoquinazolines from pyrimidines via intramolecular nucleophilic aromatic substitution of hydrogen. Chemistry of Heterocyclic Compounds, 53(10), 1156-1160. https://doi.org/10.1007/s10593-017-2188-4

Vancouver

Verbitskiy EV, Dinastiya EM, Baranova AA, Eltsov OS, Rusinov GL, Chupakhin ON et al. Synthesis of dithienoquinazolines from pyrimidines via intramolecular nucleophilic aromatic substitution of hydrogen. Chemistry of Heterocyclic Compounds. 2017 Oct 1;53(10):1156-1160. https://doi.org/10.1007/s10593-017-2188-4

Author

Verbitskiy, Egor V. ; Dinastiya, Ekaterina M. ; Baranova, Anna A. ; Eltsov, Oleg S. ; Rusinov, Gennady L. ; Chupakhin, Oleg N. ; Charushin, Valery N. / Synthesis of dithienoquinazolines from pyrimidines via intramolecular nucleophilic aromatic substitution of hydrogen. In: Chemistry of Heterocyclic Compounds. 2017 ; Vol. 53, No. 10. pp. 1156-1160.

BibTeX

@article{caeaa4ca6d054ce185b772e757de7abe,
title = "Synthesis of dithienoquinazolines from pyrimidines via intramolecular nucleophilic aromatic substitution of hydrogen",
abstract = "[Figure not available: see fulltext.] The possibility of intramolecular nucleophilic aromatic substitution of hydrogen in the series of 5-[2-(het)aryl-1-benzothiophen-3-yl]-pyrimidines was explored. A convenient method for the synthesis of [1]benzothieno-[3,2-f]thieno[2,3-h]quinazoline and [1]benzothieno-[3,2-f]thieno[3,2-h]quinazoline based on the developed SN H protocol was proposed. The energy parameters (width of the band gap, the energy of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbitals (LUMO)) of benzothieno[3,2-f]-thieno[2,3-h]quinazoline synthesized for the first time were determined based on the data of the absorption spectra and cyclic voltammetry.",
keywords = "nucleophilic aromatic substitution of hydrogen, pyrimidines, quinazolines, thienocenes",
author = "Verbitskiy, {Egor V.} and Dinastiya, {Ekaterina M.} and Baranova, {Anna A.} and Eltsov, {Oleg S.} and Rusinov, {Gennady L.} and Chupakhin, {Oleg N.} and Charushin, {Valery N.}",
year = "2017",
month = oct,
day = "1",
doi = "10.1007/s10593-017-2188-4",
language = "English",
volume = "53",
pages = "1156--1160",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer Nature",
number = "10",

}

RIS

TY - JOUR

T1 - Synthesis of dithienoquinazolines from pyrimidines via intramolecular nucleophilic aromatic substitution of hydrogen

AU - Verbitskiy, Egor V.

AU - Dinastiya, Ekaterina M.

AU - Baranova, Anna A.

AU - Eltsov, Oleg S.

AU - Rusinov, Gennady L.

AU - Chupakhin, Oleg N.

AU - Charushin, Valery N.

PY - 2017/10/1

Y1 - 2017/10/1

N2 - [Figure not available: see fulltext.] The possibility of intramolecular nucleophilic aromatic substitution of hydrogen in the series of 5-[2-(het)aryl-1-benzothiophen-3-yl]-pyrimidines was explored. A convenient method for the synthesis of [1]benzothieno-[3,2-f]thieno[2,3-h]quinazoline and [1]benzothieno-[3,2-f]thieno[3,2-h]quinazoline based on the developed SN H protocol was proposed. The energy parameters (width of the band gap, the energy of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbitals (LUMO)) of benzothieno[3,2-f]-thieno[2,3-h]quinazoline synthesized for the first time were determined based on the data of the absorption spectra and cyclic voltammetry.

AB - [Figure not available: see fulltext.] The possibility of intramolecular nucleophilic aromatic substitution of hydrogen in the series of 5-[2-(het)aryl-1-benzothiophen-3-yl]-pyrimidines was explored. A convenient method for the synthesis of [1]benzothieno-[3,2-f]thieno[2,3-h]quinazoline and [1]benzothieno-[3,2-f]thieno[3,2-h]quinazoline based on the developed SN H protocol was proposed. The energy parameters (width of the band gap, the energy of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbitals (LUMO)) of benzothieno[3,2-f]-thieno[2,3-h]quinazoline synthesized for the first time were determined based on the data of the absorption spectra and cyclic voltammetry.

KW - nucleophilic aromatic substitution of hydrogen

KW - pyrimidines

KW - quinazolines

KW - thienocenes

UR - http://www.scopus.com/inward/record.url?scp=85036498795&partnerID=8YFLogxK

U2 - 10.1007/s10593-017-2188-4

DO - 10.1007/s10593-017-2188-4

M3 - Article

AN - SCOPUS:85036498795

VL - 53

SP - 1156

EP - 1160

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 10

ER -

ID: 39452622