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Synthesis of benzo[c][1,7]naphthyridine derivatives. / Shatsauskas, Anton L.; Saibulina, Elina R.; Gatilov, Yurii V. et al.

In: Chemistry of Heterocyclic Compounds, Vol. 55, No. 11, 01.11.2019, p. 1080-1086.

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

Harvard

Shatsauskas, AL, Saibulina, ER, Gatilov, YV, Kostyuchenko, AS & Fisyuk, AS 2019, 'Synthesis of benzo[c][1,7]naphthyridine derivatives', Chemistry of Heterocyclic Compounds, vol. 55, no. 11, pp. 1080-1086. https://doi.org/10.1007/s10593-019-02581-8

APA

Shatsauskas, A. L., Saibulina, E. R., Gatilov, Y. V., Kostyuchenko, A. S., & Fisyuk, A. S. (2019). Synthesis of benzo[c][1,7]naphthyridine derivatives. Chemistry of Heterocyclic Compounds, 55(11), 1080-1086. https://doi.org/10.1007/s10593-019-02581-8

Vancouver

Shatsauskas AL, Saibulina ER, Gatilov YV, Kostyuchenko AS, Fisyuk AS. Synthesis of benzo[c][1,7]naphthyridine derivatives. Chemistry of Heterocyclic Compounds. 2019 Nov 1;55(11):1080-1086. doi: 10.1007/s10593-019-02581-8

Author

Shatsauskas, Anton L. ; Saibulina, Elina R. ; Gatilov, Yurii V. et al. / Synthesis of benzo[c][1,7]naphthyridine derivatives. In: Chemistry of Heterocyclic Compounds. 2019 ; Vol. 55, No. 11. pp. 1080-1086.

BibTeX

@article{2732989dfdfc4ebbae114efcc0354556,
title = "Synthesis of benzo[c][1,7]naphthyridine derivatives",
abstract = "Reactivity of 2-methyl-6-phenylbenzo[c][1,7]naphthyridine in alkylation, oxidation, and electrophilic substitution reactions has been studied. The reaction of 2-methyl-6-phenylbenzo[c][1,7]naphthyridines with POCl3 yielded the previously unknown 4-chloro-2-methyl-6-phenylbenzo[c][1,7]naphthyridine. Its dehalogenation and substitution of halogen by nitrogen and sulfur nucleophiles were studied.",
keywords = "alkylation, benzo[c][1,7]naphthyridine, electrophilic substitution, nucleophilic substitution, oxidation, reactivity, MARINE NATURAL-PRODUCT, CHEMISTRY, ANTAGONISTS, AAPTAMINE, ALKALOIDS",
author = "Shatsauskas, {Anton L.} and Saibulina, {Elina R.} and Gatilov, {Yurii V.} and Kostyuchenko, {Anastasia S.} and Fisyuk, {Alexander S.}",
year = "2019",
month = nov,
day = "1",
doi = "10.1007/s10593-019-02581-8",
language = "English",
volume = "55",
pages = "1080--1086",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer New York",
number = "11",

}

RIS

TY - JOUR

T1 - Synthesis of benzo[c][1,7]naphthyridine derivatives

AU - Shatsauskas, Anton L.

AU - Saibulina, Elina R.

AU - Gatilov, Yurii V.

AU - Kostyuchenko, Anastasia S.

AU - Fisyuk, Alexander S.

PY - 2019/11/1

Y1 - 2019/11/1

N2 - Reactivity of 2-methyl-6-phenylbenzo[c][1,7]naphthyridine in alkylation, oxidation, and electrophilic substitution reactions has been studied. The reaction of 2-methyl-6-phenylbenzo[c][1,7]naphthyridines with POCl3 yielded the previously unknown 4-chloro-2-methyl-6-phenylbenzo[c][1,7]naphthyridine. Its dehalogenation and substitution of halogen by nitrogen and sulfur nucleophiles were studied.

AB - Reactivity of 2-methyl-6-phenylbenzo[c][1,7]naphthyridine in alkylation, oxidation, and electrophilic substitution reactions has been studied. The reaction of 2-methyl-6-phenylbenzo[c][1,7]naphthyridines with POCl3 yielded the previously unknown 4-chloro-2-methyl-6-phenylbenzo[c][1,7]naphthyridine. Its dehalogenation and substitution of halogen by nitrogen and sulfur nucleophiles were studied.

KW - alkylation

KW - benzo[c][1,7]naphthyridine

KW - electrophilic substitution

KW - nucleophilic substitution

KW - oxidation

KW - reactivity

KW - MARINE NATURAL-PRODUCT

KW - CHEMISTRY

KW - ANTAGONISTS

KW - AAPTAMINE

KW - ALKALOIDS

UR - http://www.scopus.com/inward/record.url?scp=85076018018&partnerID=8YFLogxK

U2 - 10.1007/s10593-019-02581-8

DO - 10.1007/s10593-019-02581-8

M3 - Article

AN - SCOPUS:85076018018

VL - 55

SP - 1080

EP - 1086

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 11

ER -

ID: 22577205