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Preparation and spatial structure of methyl ether of 7 beta-methyl-D-homo-6-oxaestra-1,3,5(10),8(9)-tetraen-17a-one. / Morozkina, S. N.; Zashikhina, N. N.; Selivanov, S. I.; Shavva, A. G.

в: Russian Journal of General Chemistry, Том 84, № 9, 2014, стр. 1716-1721.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Morozkina, SN, Zashikhina, NN, Selivanov, SI & Shavva, AG 2014, 'Preparation and spatial structure of methyl ether of 7 beta-methyl-D-homo-6-oxaestra-1,3,5(10),8(9)-tetraen-17a-one', Russian Journal of General Chemistry, Том. 84, № 9, стр. 1716-1721. https://doi.org/10.1134/S1070363214090138

APA

Morozkina, S. N., Zashikhina, N. N., Selivanov, S. I., & Shavva, A. G. (2014). Preparation and spatial structure of methyl ether of 7 beta-methyl-D-homo-6-oxaestra-1,3,5(10),8(9)-tetraen-17a-one. Russian Journal of General Chemistry, 84(9), 1716-1721. https://doi.org/10.1134/S1070363214090138

Vancouver

Morozkina SN, Zashikhina NN, Selivanov SI, Shavva AG. Preparation and spatial structure of methyl ether of 7 beta-methyl-D-homo-6-oxaestra-1,3,5(10),8(9)-tetraen-17a-one. Russian Journal of General Chemistry. 2014;84(9):1716-1721. https://doi.org/10.1134/S1070363214090138

Author

Morozkina, S. N. ; Zashikhina, N. N. ; Selivanov, S. I. ; Shavva, A. G. / Preparation and spatial structure of methyl ether of 7 beta-methyl-D-homo-6-oxaestra-1,3,5(10),8(9)-tetraen-17a-one. в: Russian Journal of General Chemistry. 2014 ; Том 84, № 9. стр. 1716-1721.

BibTeX

@article{e65a7681c82a4f0a9b5149e8d5286c03,
title = "Preparation and spatial structure of methyl ether of 7 beta-methyl-D-homo-6-oxaestra-1,3,5(10),8(9)-tetraen-17a-one",
abstract = "Procedure of preparation of 7 beta-methyl-D-homo-6-oxa-1,3,5(10),8,(9)-estratetraen-17a-one methyl ether has been developed; the product conformation in the solution has been studied by NMR spectroscopy. Comparison of the experimental data with simulation of similar compounds docking into the ligand-binding pocket of the estrogens alpha-receptor has suggested that such steroids are promising for preparation of biologically active substances whose action would not be mediated by the estrogens receptors.",
author = "Morozkina, {S. N.} and Zashikhina, {N. N.} and Selivanov, {S. I.} and Shavva, {A. G.}",
year = "2014",
doi = "10.1134/S1070363214090138",
language = "English",
volume = "84",
pages = "1716--1721",
journal = "Russian Journal of General Chemistry",
issn = "1070-3632",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "9",

}

RIS

TY - JOUR

T1 - Preparation and spatial structure of methyl ether of 7 beta-methyl-D-homo-6-oxaestra-1,3,5(10),8(9)-tetraen-17a-one

AU - Morozkina, S. N.

AU - Zashikhina, N. N.

AU - Selivanov, S. I.

AU - Shavva, A. G.

PY - 2014

Y1 - 2014

N2 - Procedure of preparation of 7 beta-methyl-D-homo-6-oxa-1,3,5(10),8,(9)-estratetraen-17a-one methyl ether has been developed; the product conformation in the solution has been studied by NMR spectroscopy. Comparison of the experimental data with simulation of similar compounds docking into the ligand-binding pocket of the estrogens alpha-receptor has suggested that such steroids are promising for preparation of biologically active substances whose action would not be mediated by the estrogens receptors.

AB - Procedure of preparation of 7 beta-methyl-D-homo-6-oxa-1,3,5(10),8,(9)-estratetraen-17a-one methyl ether has been developed; the product conformation in the solution has been studied by NMR spectroscopy. Comparison of the experimental data with simulation of similar compounds docking into the ligand-binding pocket of the estrogens alpha-receptor has suggested that such steroids are promising for preparation of biologically active substances whose action would not be mediated by the estrogens receptors.

U2 - 10.1134/S1070363214090138

DO - 10.1134/S1070363214090138

M3 - Article

VL - 84

SP - 1716

EP - 1721

JO - Russian Journal of General Chemistry

JF - Russian Journal of General Chemistry

SN - 1070-3632

IS - 9

ER -

ID: 7065420