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Cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with amidines. New synthesis of isoquinolines. / Dar'in, D. V.; Selivanov, S. I.; Lobanov, P. S.; Potekhin, A. A.

в: Chemistry of Heterocyclic Compounds, Том 40, № 7, 01.07.2004, стр. 888-894.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Dar'in, DV, Selivanov, SI, Lobanov, PS & Potekhin, AA 2004, 'Cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with amidines. New synthesis of isoquinolines', Chemistry of Heterocyclic Compounds, Том. 40, № 7, стр. 888-894. https://doi.org/10.1023/B:COHC.0000044571.89322.4e

APA

Vancouver

Author

Dar'in, D. V. ; Selivanov, S. I. ; Lobanov, P. S. ; Potekhin, A. A. / Cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with amidines. New synthesis of isoquinolines. в: Chemistry of Heterocyclic Compounds. 2004 ; Том 40, № 7. стр. 888-894.

BibTeX

@article{dbb4923cfec449858aab57235b5ec62b,
title = "Cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with amidines. New synthesis of isoquinolines",
abstract = "The direction of the cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with five amidines having α-hydrogen atoms has been studied. It was established that depending on the structure of the amidine the main products of the reaction may be not only quinazolines but also 3-aminoisoquinolines. A new convenient route has been found for the synthesis of 3-aminoisoquinolines consisting of the cyclocondensation of α-acylacetamidines with 2-fluoro-5-nitrobenzaldehyde.",
keywords = "2-fluoro-5- nitrobenzaldehyde, amidines as N,N- and C,N-dinucleophiles, cyclocondensation, isoquinolines",
author = "Dar'in, {D. V.} and Selivanov, {S. I.} and Lobanov, {P. S.} and Potekhin, {A. A.}",
year = "2004",
month = jul,
day = "1",
doi = "10.1023/B:COHC.0000044571.89322.4e",
language = "English",
volume = "40",
pages = "888--894",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer Nature",
number = "7",

}

RIS

TY - JOUR

T1 - Cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with amidines. New synthesis of isoquinolines

AU - Dar'in, D. V.

AU - Selivanov, S. I.

AU - Lobanov, P. S.

AU - Potekhin, A. A.

PY - 2004/7/1

Y1 - 2004/7/1

N2 - The direction of the cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with five amidines having α-hydrogen atoms has been studied. It was established that depending on the structure of the amidine the main products of the reaction may be not only quinazolines but also 3-aminoisoquinolines. A new convenient route has been found for the synthesis of 3-aminoisoquinolines consisting of the cyclocondensation of α-acylacetamidines with 2-fluoro-5-nitrobenzaldehyde.

AB - The direction of the cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with five amidines having α-hydrogen atoms has been studied. It was established that depending on the structure of the amidine the main products of the reaction may be not only quinazolines but also 3-aminoisoquinolines. A new convenient route has been found for the synthesis of 3-aminoisoquinolines consisting of the cyclocondensation of α-acylacetamidines with 2-fluoro-5-nitrobenzaldehyde.

KW - 2-fluoro-5- nitrobenzaldehyde

KW - amidines as N,N- and C,N-dinucleophiles

KW - cyclocondensation

KW - isoquinolines

UR - http://www.scopus.com/inward/record.url?scp=6344263398&partnerID=8YFLogxK

U2 - 10.1023/B:COHC.0000044571.89322.4e

DO - 10.1023/B:COHC.0000044571.89322.4e

M3 - Article

AN - SCOPUS:6344263398

VL - 40

SP - 888

EP - 894

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 7

ER -

ID: 36262537