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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.

In: Chemistry of Natural Compounds, Vol. 58, No. 2, 01.03.2022, p. 290-296.

Research output: Contribution to journal › Article › peer-review

Harvard

Shpatov, AV, Zakharova, SS & Popov, SA 2022, 'Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles', Chemistry of Natural Compounds, vol. 58, no. 2, pp. 290-296. https://doi.org/10.1007/s10600-022-03662-5

APA

Shpatov, A. V., Zakharova, S. S., & Popov, S. A. (2022). Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles. Chemistry of Natural Compounds, 58(2), 290-296. https://doi.org/10.1007/s10600-022-03662-5

Vancouver

Shpatov AV, Zakharova SS, Popov SA. Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles. Chemistry of Natural Compounds. 2022 Mar 1;58(2):290-296. Epub 2022 Mar. doi: 10.1007/s10600-022-03662-5

Author

Shpatov, A. V. ; Zakharova, S. S. ; Popov, S. A. / Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles. In: Chemistry of Natural Compounds. 2022 ; Vol. 58, No. 2. pp. 290-296.

BibTeX

@article{03f958645dae48d5b85ee46ac84fc184,
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.",
year = "2022",
month = mar,
day = "1",
doi = "10.1007/s10600-022-03662-5",
language = "English",
volume = "58",
pages = "290--296",
journal = "Chemistry of Natural Compounds",
issn = "0009-3130",
publisher = "Springer New York",
number = "2",

}

RIS

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

UR - http://www.scopus.com/inward/record.url?scp=85129634435&partnerID=8YFLogxK

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 -

ID: 36075688