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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.

в: Chemistry of Heterocyclic Compounds, Том 53, № 10, 01.10.2017, стр. 1156-1160.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

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, Том. 53, № 10, стр. 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 и пр. Synthesis of dithienoquinazolines from pyrimidines via intramolecular nucleophilic aromatic substitution of hydrogen. Chemistry of Heterocyclic Compounds. 2017 Окт. 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. в: Chemistry of Heterocyclic Compounds. 2017 ; Том 53, № 10. стр. 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