Research output: Contribution to journal › Article › peer-review
2-Hydroxy-3-octyloxybenzaldehyde. / Novoselova, Julia V.; Vereshchagin, Anatoliy A.; Kalnin, Arseniy Y.; Lukyanov, Daniil A.; Levin, Oleg V.
In: MolBank, Vol. 2021, No. 3, M1264, 03.08.2021.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - 2-Hydroxy-3-octyloxybenzaldehyde
AU - Novoselova, Julia V.
AU - Vereshchagin, Anatoliy A.
AU - Kalnin, Arseniy Y.
AU - Lukyanov, Daniil A.
AU - Levin, Oleg V.
N1 - Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/8/3
Y1 - 2021/8/3
N2 - Herein, we report the chromatography-free synthesis of 2-hydroxy-3-octyloxybenzaldehyde by the alkylation of 2,3-dihydroxybenzaldehyde as a promising precursor for new SalEn-type complexes with transition metals. The structure of the product is elucidated by means of 1H and 13C-NMR spectra, high-resolution mass spectrometry with electrospray ionization (ESI-HRMS) and Fourier-transform infrared spectroscopy (FTIR).
AB - Herein, we report the chromatography-free synthesis of 2-hydroxy-3-octyloxybenzaldehyde by the alkylation of 2,3-dihydroxybenzaldehyde as a promising precursor for new SalEn-type complexes with transition metals. The structure of the product is elucidated by means of 1H and 13C-NMR spectra, high-resolution mass spectrometry with electrospray ionization (ESI-HRMS) and Fourier-transform infrared spectroscopy (FTIR).
KW - 2-hydroxy-3-octylbenzaldehyde
KW - Alkylation
KW - SalEn precursor
KW - Schiff base
KW - DESIGN
KW - COMPLEXES
KW - NI-SALEN
KW - OXYGEN
KW - NICKEL
KW - REDUCTION
KW - alkylation
KW - ELECTROCHEMICAL SENSOR
KW - CATALYSTS
UR - http://www.scopus.com/inward/record.url?scp=85112280880&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/9a697ae1-7cb8-379d-8897-32eb8969060e/
U2 - 10.3390/M1264
DO - 10.3390/M1264
M3 - Article
AN - SCOPUS:85112280880
VL - 2021
JO - MolBank
JF - MolBank
SN - 1422-8599
IS - 3
M1 - M1264
ER -
ID: 84798169