Research output: Contribution to journal › Article › peer-review
Synthesis of 3-and 2,3-substituted pyrazolo[1,5-a][1,10]phenanthrolines. / Sannikova, Viktoriya; Filippov, Igor R.; Karmatskikh, Oleg Yu et al.
In: Chemistry of Heterocyclic Compounds, Vol. 56, No. 8, 01.08.2020, p. 1042-1047.Research output: Contribution to journal › Article › peer-review
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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