1H,13C and15N NMR spectroscopy and tautomerism of nitrobenzotriazoles
Publication type: Journal Article
Publication date: 2008-11-28
scimago Q3
wos Q3
SJR: 0.360
CiteScore: 4.1
Impact factor: 1.4
ISSN: 07491581, 1097458X
DOI:
10.1002/mrc.2366
PubMed ID:
19040197
General Chemistry
General Materials Science
Abstract
Benzotriazole nitro derivatives were prepared by nitration of the corresponding benzotriazoles and by methylation or cyclization of appropriate nitro-1,2-phenylenediamines. Structures and tautomerism of the nitrobenzotriazoles were studied by multinuclear (1)H, (13)C, (15)N, and 2D NMR spectroscopy and quantum chemistry.
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27
Total citations:
27
Citations from 2024:
2
(7.41%)
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MLA
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GOST
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Larina L. I., Milata V. 1H,13C and15N NMR spectroscopy and tautomerism of nitrobenzotriazoles // Magnetic Resonance in Chemistry. 2008. Vol. 47. No. 2. pp. 142-148.
GOST all authors (up to 50)
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Larina L. I., Milata V. 1H,13C and15N NMR spectroscopy and tautomerism of nitrobenzotriazoles // Magnetic Resonance in Chemistry. 2008. Vol. 47. No. 2. pp. 142-148.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/mrc.2366
UR - https://doi.org/10.1002/mrc.2366
TI - 1H,13C and15N NMR spectroscopy and tautomerism of nitrobenzotriazoles
T2 - Magnetic Resonance in Chemistry
AU - Larina, Lyudmila I.
AU - Milata, Viktor
PY - 2008
DA - 2008/11/28
PB - Wiley
SP - 142-148
IS - 2
VL - 47
PMID - 19040197
SN - 0749-1581
SN - 1097-458X
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2008_Larina,
author = {Lyudmila I. Larina and Viktor Milata},
title = {1H,13C and15N NMR spectroscopy and tautomerism of nitrobenzotriazoles},
journal = {Magnetic Resonance in Chemistry},
year = {2008},
volume = {47},
publisher = {Wiley},
month = {nov},
url = {https://doi.org/10.1002/mrc.2366},
number = {2},
pages = {142--148},
doi = {10.1002/mrc.2366}
}
Cite this
MLA
Copy
Larina, Lyudmila I., and Viktor Milata. “1H,13C and15N NMR spectroscopy and tautomerism of nitrobenzotriazoles.” Magnetic Resonance in Chemistry, vol. 47, no. 2, Nov. 2008, pp. 142-148. https://doi.org/10.1002/mrc.2366.