Hydroacridines and related compounds. 22. Synthesis of compound with 2,6-epidioxypiperidine structure
Publication type: Journal Article
Publication date: 1985-01-01
scimago Q4
wos Q4
SJR: 0.243
CiteScore: 2.7
Impact factor: 1.0
ISSN: 00093122, 15738353
Organic Chemistry
Abstract
The addition of hydrogen peroxide to a series of 1,4-dihydropyridine derivatives proceeds with the formation of derivatives of 6,7-dioxa-8-azabicyclo[3.2.1]octane. Such compounds may be obtained by the reaction of alicyclic 1,5-diketones with amines and hydrogen peroxide.
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Shumakov S. A., Kaminskii V. A., Tilichenko M. N. Hydroacridines and related compounds. 22. Synthesis of compound with 2,6-epidioxypiperidine structure // Chemistry of Heterocyclic Compounds. 1985. Vol. 21. No. 1. pp. 72-77.
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Shumakov S. A., Kaminskii V. A., Tilichenko M. N. Hydroacridines and related compounds. 22. Synthesis of compound with 2,6-epidioxypiperidine structure // Chemistry of Heterocyclic Compounds. 1985. Vol. 21. No. 1. pp. 72-77.
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TY - JOUR
DO - 10.1007/BF00505905
UR - https://doi.org/10.1007/BF00505905
TI - Hydroacridines and related compounds. 22. Synthesis of compound with 2,6-epidioxypiperidine structure
T2 - Chemistry of Heterocyclic Compounds
AU - Shumakov, S A
AU - Kaminskii, V A
AU - Tilichenko, M N
PY - 1985
DA - 1985/01/01
PB - Springer Nature
SP - 72-77
IS - 1
VL - 21
SN - 0009-3122
SN - 1573-8353
ER -
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BibTex (up to 50 authors)
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@article{1985_Shumakov,
author = {S A Shumakov and V A Kaminskii and M N Tilichenko},
title = {Hydroacridines and related compounds. 22. Synthesis of compound with 2,6-epidioxypiperidine structure},
journal = {Chemistry of Heterocyclic Compounds},
year = {1985},
volume = {21},
publisher = {Springer Nature},
month = {jan},
url = {https://doi.org/10.1007/BF00505905},
number = {1},
pages = {72--77},
doi = {10.1007/BF00505905}
}
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MLA
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Shumakov, S. A., et al. “Hydroacridines and related compounds. 22. Synthesis of compound with 2,6-epidioxypiperidine structure.” Chemistry of Heterocyclic Compounds, vol. 21, no. 1, Jan. 1985, pp. 72-77. https://doi.org/10.1007/BF00505905.