Home / Publications / A simple preparation of ω-hydroxydienoic fatty acids with double-bond positional isomerism

A simple preparation of ω-hydroxydienoic fatty acids with double-bond positional isomerism

Igor Vladimirovich Ivanov 1
Igor Vladimirovich Ivanov
, 
Galina Ivanovna Myagkova 1
Galina Ivanovna Myagkova
, 
Hartmut Kuhn 2
Hartmut Kuhn
10.1070/MC1998v008n06ABEH001031
Published 1998-12-16
Communication , Volume 8, Issue 6, 222-224
1
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Ivanov I. V., Myagkova G. I., Kuhn H. A simple preparation of ω-hydroxydienoic fatty acids with double-bond positional isomerism // Mendeleev Communications. 1998. Vol. 8. No. 6. pp. 222-224.
GOST all authors (up to 50) Copy
Ivanov I. V., Myagkova G. I., Kuhn H. A simple preparation of ω-hydroxydienoic fatty acids with double-bond positional isomerism // Mendeleev Communications. 1998. Vol. 8. No. 6. pp. 222-224.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1070/MC1998v008n06ABEH001031
UR - https://mendcomm.colab.ws/publications/10.1070/MC1998v008n06ABEH001031
TI - A simple preparation of ω-hydroxydienoic fatty acids with double-bond positional isomerism
T2 - Mendeleev Communications
AU - Ivanov, Igor Vladimirovich
AU - Myagkova, Galina Ivanovna
AU - Kuhn, Hartmut
PY - 1998
DA - 1998/12/16
PB - Mendeleev Communications
SP - 222-224
IS - 6
VL - 8
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{1998_Ivanov,
author = {Igor Vladimirovich Ivanov and Galina Ivanovna Myagkova and Hartmut Kuhn},
title = {A simple preparation of ω-hydroxydienoic fatty acids with double-bond positional isomerism},
journal = {Mendeleev Communications},
year = {1998},
volume = {8},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1998v008n06ABEH001031},
number = {6},
pages = {222--224},
doi = {10.1070/MC1998v008n06ABEH001031}
}
MLA
Cite this
MLA Copy
Ivanov, Igor Vladimirovich, et al. “A simple preparation of ω-hydroxydienoic fatty acids with double-bond positional isomerism.” Mendeleev Communications, vol. 8, no. 6, Dec. 1998, pp. 222-224. https://mendcomm.colab.ws/publications/10.1070/MC1998v008n06ABEH001031.

Abstract

A set of new regioisomeric ω-hydroxydienoic fatty acids has been prepared via a three-step procedure involving the methylation of ω-carboxydienoic fatty acids followed by the NaBH4 reduction of a mixture of the resulting monomethyl esters and HPLC separation.

References

4.
The structure of mammalian 15-lipoxygenase reveals similarity to the lipases and the determinants of substrate specificity
Gillmor S.A., Villaseñor A., Fletterick R., Sigal E., Browner M.F.
Nature Structural Biology, 1997
5.
Defining the Arachidonic Acid Binding Site of Human 15-Lipoxygenase
Gan Q., Browner M.F., Sloane D.L., Sigal E.
Journal of Biological Chemistry, 1996
6.
Phenylalanine 353 is a primary determinant for the positional specificity of mammalian 15-lipoxygenases.
Borngräber S., Kuban R., Anton M., Kühn H.
Journal of Molecular Biology, 1996
8.
10.1070/MC1998v008n06ABEH001031_bib8
Ivanov
Bioorg. Khim., 1997
9.
10.1070/MC1998v008n06ABEH001031_bib9
Ivanov
Bioorg. Khim., 1998