Synthesis and Structural Studies of N-Heterocyclic Schiff Bases of Allobetulamine
Publication type: Journal Article
Publication date: 2022-03-01
scimago Q3
wos Q4
SJR: 0.296
CiteScore: 1.3
Impact factor: 0.9
ISSN: 00093130, 15738388
General Chemistry
General Biochemistry, Genetics and Molecular Biology
Plant Science
Abstract
Triterpene Schiff bases 2–5 were prepared for the first time by reacting N-heterocyclic carbaldehydes with β-allobetulamine. Their structures were confirmed using 1H NMR and 13C NMR spectra and 2D experiments. The structure of 5 was also proved by an X-ray crystal structure analysis.
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Denisov M. S. et al. Synthesis and Structural Studies of N-Heterocyclic Schiff Bases of Allobetulamine // Chemistry of Natural Compounds. 2022. Vol. 58. No. 2. pp. 307-311.
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Denisov M. S., Dmitriev M. V., Gagarskikh O. N., Glushkov V. A. Synthesis and Structural Studies of N-Heterocyclic Schiff Bases of Allobetulamine // Chemistry of Natural Compounds. 2022. Vol. 58. No. 2. pp. 307-311.
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TY - JOUR
DO - 10.1007/s10600-022-03665-2
UR - https://doi.org/10.1007/s10600-022-03665-2
TI - Synthesis and Structural Studies of N-Heterocyclic Schiff Bases of Allobetulamine
T2 - Chemistry of Natural Compounds
AU - Denisov, M S
AU - Dmitriev, M V
AU - Gagarskikh, O N
AU - Glushkov, V A
PY - 2022
DA - 2022/03/01
PB - Springer Nature
SP - 307-311
IS - 2
VL - 58
SN - 0009-3130
SN - 1573-8388
ER -
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BibTex (up to 50 authors)
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@article{2022_Denisov,
author = {M S Denisov and M V Dmitriev and O N Gagarskikh and V A Glushkov},
title = {Synthesis and Structural Studies of N-Heterocyclic Schiff Bases of Allobetulamine},
journal = {Chemistry of Natural Compounds},
year = {2022},
volume = {58},
publisher = {Springer Nature},
month = {mar},
url = {https://doi.org/10.1007/s10600-022-03665-2},
number = {2},
pages = {307--311},
doi = {10.1007/s10600-022-03665-2}
}
Cite this
MLA
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Denisov, M. S., et al. “Synthesis and Structural Studies of N-Heterocyclic Schiff Bases of Allobetulamine.” Chemistry of Natural Compounds, vol. 58, no. 2, Mar. 2022, pp. 307-311. https://doi.org/10.1007/s10600-022-03665-2.
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