Standard

Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines. / Sannikova, Viktoriya; Filippov, Igor R.; Karmatskikh, Oleg Yu и др.

в: Chemistry of Heterocyclic Compounds, Том 56, № 8, 01.08.2020, стр. 1042-1047.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Sannikova, V, Filippov, IR, Karmatskikh, OY, Panfilov, M, Andreev, RV & Vorob’ev, AY 2020, 'Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines', Chemistry of Heterocyclic Compounds, Том. 56, № 8, стр. 1042-1047. https://doi.org/10.1007/s10593-020-02772-8

APA

Sannikova, V., Filippov, I. R., Karmatskikh, O. Y., Panfilov, M., Andreev, R. V., & Vorob’ev, A. Y. (2020). Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines. Chemistry of Heterocyclic Compounds, 56(8), 1042-1047. https://doi.org/10.1007/s10593-020-02772-8

Vancouver

Sannikova V, Filippov IR, Karmatskikh OY, Panfilov M, Andreev RV, Vorob’ev AY. Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines. Chemistry of Heterocyclic Compounds. 2020 авг. 1;56(8):1042-1047. doi: 10.1007/s10593-020-02772-8

Author

Sannikova, Viktoriya ; Filippov, Igor R. ; Karmatskikh, Oleg Yu и др. / Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines. в: Chemistry of Heterocyclic Compounds. 2020 ; Том 56, № 8. стр. 1042-1047.

BibTeX

@article{938c0379d52e4d6b885df0d2b0e63d56,
title = "Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines",
abstract = "The reaction of N-amino-1,10-phenanthrolinium mesitylenesulfonate with acceptor-substituted alkenes in the K2CO3–DMSO system gave 3- and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines. A wide range of alkenes enter into this reaction; however, in the case of nitro derivatives, complex mixtures of products were formed.",
keywords = "1,10-phenanthroline, 1,3-dipolar cycloaddition, acceptor alkenes, N-aminophenanthrolinium cation, pyrazolo[1,5-a][1,10]phenanthrolines",
author = "Viktoriya Sannikova and Filippov, {Igor R.} and Karmatskikh, {Oleg Yu} and Mikhail Panfilov and Andreev, {Rodion V.} and Vorob{\textquoteright}ev, {Aleksey Yu}",
note = "Publisher Copyright: {\textcopyright} 2020, Springer Science+Business Media, LLC, part of Springer Nature. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.",
year = "2020",
month = aug,
day = "1",
doi = "10.1007/s10593-020-02772-8",
language = "English",
volume = "56",
pages = "1042--1047",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer New York",
number = "8",

}

RIS

TY - JOUR

T1 - Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines

AU - Sannikova, Viktoriya

AU - Filippov, Igor R.

AU - Karmatskikh, Oleg Yu

AU - Panfilov, Mikhail

AU - Andreev, Rodion V.

AU - Vorob’ev, Aleksey Yu

N1 - Publisher Copyright: © 2020, Springer Science+Business Media, LLC, part of Springer Nature. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.

PY - 2020/8/1

Y1 - 2020/8/1

N2 - The reaction of N-amino-1,10-phenanthrolinium mesitylenesulfonate with acceptor-substituted alkenes in the K2CO3–DMSO system gave 3- and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines. A wide range of alkenes enter into this reaction; however, in the case of nitro derivatives, complex mixtures of products were formed.

AB - The reaction of N-amino-1,10-phenanthrolinium mesitylenesulfonate with acceptor-substituted alkenes in the K2CO3–DMSO system gave 3- and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines. A wide range of alkenes enter into this reaction; however, in the case of nitro derivatives, complex mixtures of products were formed.

KW - 1,10-phenanthroline

KW - 1,3-dipolar cycloaddition

KW - acceptor alkenes

KW - N-aminophenanthrolinium cation

KW - pyrazolo[1,5-a][1,10]phenanthrolines

UR - http://www.scopus.com/inward/record.url?scp=85091432336&partnerID=8YFLogxK

U2 - 10.1007/s10593-020-02772-8

DO - 10.1007/s10593-020-02772-8

M3 - Article

AN - SCOPUS:85091432336

VL - 56

SP - 1042

EP - 1047

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 8

ER -

ID: 25651278