Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles

A. V. Shpatov; S. S. Zakharova; S. A. Popov

doi:10.1007/s10600-022-03662-5

Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles

A. V. Shpatov, S. S. Zakharova, S. A. Popov

Факультет естественных наук

Результат исследования: Научные публикации в периодических изданиях › статья › рецензирование

Аннотация

New hybrid compounds of abietic acid with 2-thione-, 2-alkylthio-, and 2-alkylamino-1,3,4-oxadiazole fragments at various distances from the diterpene skeleton were synthesized in situ via cyclization in acidic medium of intermediate dithiocarbamates or cyclodesulfurization of intermediate acylthiosemicarbazides through the action of Hg(OAc)₂.

Язык оригинала	английский
Страницы (с-по)	290-296
Число страниц	7
Журнал	Chemistry of Natural Compounds
Том	58
Номер выпуска	2
Ранняя дата в режиме онлайн	мар. 2022
DOI	https://doi.org/10.1007/s10600-022-03662-5
Состояние	Опубликовано - 1 мар. 2022

Предметные области OECD FOS+WOS

1.06 БИОЛОГИЧЕСКИЕ НАУКИ

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10.1007/s10600-022-03662-5

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title = "Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles",

abstract = "New hybrid compounds of abietic acid with 2-thione-, 2-alkylthio-, and 2-alkylamino-1,3,4-oxadiazole fragments at various distances from the diterpene skeleton were synthesized in situ via cyclization in acidic medium of intermediate dithiocarbamates or cyclodesulfurization of intermediate acylthiosemicarbazides through the action of Hg(OAc)2.",

keywords = "2-substituted 1,3,4-oxadiazoles, abietic acid, acylthiosemicarbazides, cyclization, cyclodesulfurization, dithiocarbamates",

author = "Shpatov, {A. V.} and Zakharova, {S. S.} and Popov, {S. A.}",

note = "Funding Information: The work was performed under State Task 1021051503128-9-1.4.1. We thank Khimiya Common Use Center, SB, RAS, for performing the spectral and analytical measurements. Publisher Copyright: {\textcopyright} 2022, Springer Science+Business Media, LLC, part of Springer Nature.",

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doi = "10.1007/s10600-022-03662-5",

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Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles. / Shpatov, A. V.; Zakharova, S. S.; Popov, S. A.

В: Chemistry of Natural Compounds, Том 58, № 2, 01.03.2022, стр. 290-296.

Результат исследования: Научные публикации в периодических изданиях › статья › рецензирование

TY - JOUR

T1 - Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles

AU - Shpatov, A. V.

AU - Zakharova, S. S.

AU - Popov, S. A.

N1 - Funding Information: The work was performed under State Task 1021051503128-9-1.4.1. We thank Khimiya Common Use Center, SB, RAS, for performing the spectral and analytical measurements. Publisher Copyright: © 2022, Springer Science+Business Media, LLC, part of Springer Nature.

PY - 2022/3/1

Y1 - 2022/3/1

N2 - New hybrid compounds of abietic acid with 2-thione-, 2-alkylthio-, and 2-alkylamino-1,3,4-oxadiazole fragments at various distances from the diterpene skeleton were synthesized in situ via cyclization in acidic medium of intermediate dithiocarbamates or cyclodesulfurization of intermediate acylthiosemicarbazides through the action of Hg(OAc)2.

AB - New hybrid compounds of abietic acid with 2-thione-, 2-alkylthio-, and 2-alkylamino-1,3,4-oxadiazole fragments at various distances from the diterpene skeleton were synthesized in situ via cyclization in acidic medium of intermediate dithiocarbamates or cyclodesulfurization of intermediate acylthiosemicarbazides through the action of Hg(OAc)2.

KW - 2-substituted 1,3,4-oxadiazoles

KW - abietic acid

KW - acylthiosemicarbazides

KW - cyclization

KW - cyclodesulfurization

KW - dithiocarbamates

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UR - https://www.mendeley.com/catalogue/ff4d812e-f632-3de9-8d21-ca1f0a57c973/

U2 - 10.1007/s10600-022-03662-5

DO - 10.1007/s10600-022-03662-5

M3 - Article

AN - SCOPUS:85129634435

VL - 58

SP - 290

EP - 296

JO - Chemistry of Natural Compounds

JF - Chemistry of Natural Compounds

SN - 0009-3130

IS - 2

ER -

Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles

Аннотация

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