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Synthesis of lappaconitine N-oxide under microwave activation. / Pankrushina, Natalia A.; Rakhmetali, Kymbat B.

в: Chemistry of Heterocyclic Compounds, Том 52, № 11, 01.11.2016, стр. 970-972.

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

Harvard

Pankrushina, NA & Rakhmetali, KB 2016, 'Synthesis of lappaconitine N-oxide under microwave activation', Chemistry of Heterocyclic Compounds, Том. 52, № 11, стр. 970-972. https://doi.org/10.1007/s10593-017-1995-y

APA

Pankrushina, N. A., & Rakhmetali, K. B. (2016). Synthesis of lappaconitine N-oxide under microwave activation. Chemistry of Heterocyclic Compounds, 52(11), 970-972. https://doi.org/10.1007/s10593-017-1995-y

Vancouver

Pankrushina NA, Rakhmetali KB. Synthesis of lappaconitine N-oxide under microwave activation. Chemistry of Heterocyclic Compounds. 2016 нояб. 1;52(11):970-972. doi: 10.1007/s10593-017-1995-y

Author

Pankrushina, Natalia A. ; Rakhmetali, Kymbat B. / Synthesis of lappaconitine N-oxide under microwave activation. в: Chemistry of Heterocyclic Compounds. 2016 ; Том 52, № 11. стр. 970-972.

BibTeX

@article{5e5b8fd6fa394d2b817b68b3fbda2411,
title = "Synthesis of lappaconitine N-oxide under microwave activation",
abstract = "Lappaconitine N-oxide was obtained in high yield via oxidation of lappaconitine with OxoneA (R) in H2O-MeCN media under the conditions of microwave activation.",
keywords = "lappaconitine, microwave activation, Oxone{\textregistered}, Oxone (R), ALKALOIDS",
author = "Pankrushina, {Natalia A.} and Rakhmetali, {Kymbat B.}",
year = "2016",
month = nov,
day = "1",
doi = "10.1007/s10593-017-1995-y",
language = "English",
volume = "52",
pages = "970--972",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer New York",
number = "11",

}

RIS

TY - JOUR

T1 - Synthesis of lappaconitine N-oxide under microwave activation

AU - Pankrushina, Natalia A.

AU - Rakhmetali, Kymbat B.

PY - 2016/11/1

Y1 - 2016/11/1

N2 - Lappaconitine N-oxide was obtained in high yield via oxidation of lappaconitine with OxoneA (R) in H2O-MeCN media under the conditions of microwave activation.

AB - Lappaconitine N-oxide was obtained in high yield via oxidation of lappaconitine with OxoneA (R) in H2O-MeCN media under the conditions of microwave activation.

KW - lappaconitine

KW - microwave activation

KW - Oxone®

KW - Oxone (R)

KW - ALKALOIDS

UR - http://www.scopus.com/inward/record.url?scp=85008601936&partnerID=8YFLogxK

U2 - 10.1007/s10593-017-1995-y

DO - 10.1007/s10593-017-1995-y

M3 - Article

VL - 52

SP - 970

EP - 972

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 11

ER -

ID: 10316587