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Synthesis and properties of 2-cyanoethoxy derivatives of dammarane triterpenoids. / Kaledina, A.S.; Zorina, A.D.; Zarubaev, V.V.; Anokhina, V.V.; Erkhitueva, E.B.; Trifonov, R.E.

в: Russian Journal of Organic Chemistry, № 11, 2015, стр. 1627-1632.

Результаты исследований: Научные публикации в периодических изданиях › статья

Harvard

Kaledina, AS, Zorina, AD, Zarubaev, VV, Anokhina, VV, Erkhitueva, EB & Trifonov, RE 2015, 'Synthesis and properties of 2-cyanoethoxy derivatives of dammarane triterpenoids', Russian Journal of Organic Chemistry, № 11, стр. 1627-1632. https://doi.org/10.1134/S1070428015110184

APA

Kaledina, A. S., Zorina, A. D., Zarubaev, V. V., Anokhina, V. V., Erkhitueva, E. B., & Trifonov, R. E. (2015). Synthesis and properties of 2-cyanoethoxy derivatives of dammarane triterpenoids. Russian Journal of Organic Chemistry, (11), 1627-1632. https://doi.org/10.1134/S1070428015110184

Vancouver

Kaledina AS, Zorina AD, Zarubaev VV, Anokhina VV, Erkhitueva EB, Trifonov RE. Synthesis and properties of 2-cyanoethoxy derivatives of dammarane triterpenoids. Russian Journal of Organic Chemistry. 2015;(11):1627-1632. https://doi.org/10.1134/S1070428015110184

Author

Kaledina, A.S. ; Zorina, A.D. ; Zarubaev, V.V. ; Anokhina, V.V. ; Erkhitueva, E.B. ; Trifonov, R.E. / Synthesis and properties of 2-cyanoethoxy derivatives of dammarane triterpenoids. в: Russian Journal of Organic Chemistry. 2015 ; № 11. стр. 1627-1632.

BibTeX

@article{ad0ed14b6f0046b7b792d54df1c8ad69,
title = "Synthesis and properties of 2-cyanoethoxy derivatives of dammarane triterpenoids",
abstract = "{\textcopyright} 2015 Pleiades Publishing, Ltd.Cyanoethylation of dammaran-3β-ols and 3-oxime dammarene, semisynthetic derivatives of the natural dipterocarpol, afforded a series of new dammarane triterpenoids containing 2-cyanoethoxy fragment at the carbon atom in the position 3 of the tetracyclic scaffold. A notable antiviral activity was found in 20(S)-3-[(2-cyanoethoxy)imino]-dammar-24-en-20-ol and 20(S)-3-O-(2-cyanoethyl)-25,26,27-trinor-20,24-olidedammarane.",
author = "A.S. Kaledina and A.D. Zorina and V.V. Zarubaev and V.V. Anokhina and E.B. Erkhitueva and R.E. Trifonov",
year = "2015",
doi = "10.1134/S1070428015110184",
language = "English",
pages = "1627--1632",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "11",

}

RIS

TY - JOUR

T1 - Synthesis and properties of 2-cyanoethoxy derivatives of dammarane triterpenoids

AU - Kaledina, A.S.

AU - Zorina, A.D.

AU - Zarubaev, V.V.

AU - Anokhina, V.V.

AU - Erkhitueva, E.B.

AU - Trifonov, R.E.

PY - 2015

Y1 - 2015

N2 - © 2015 Pleiades Publishing, Ltd.Cyanoethylation of dammaran-3β-ols and 3-oxime dammarene, semisynthetic derivatives of the natural dipterocarpol, afforded a series of new dammarane triterpenoids containing 2-cyanoethoxy fragment at the carbon atom in the position 3 of the tetracyclic scaffold. A notable antiviral activity was found in 20(S)-3-[(2-cyanoethoxy)imino]-dammar-24-en-20-ol and 20(S)-3-O-(2-cyanoethyl)-25,26,27-trinor-20,24-olidedammarane.

AB - © 2015 Pleiades Publishing, Ltd.Cyanoethylation of dammaran-3β-ols and 3-oxime dammarene, semisynthetic derivatives of the natural dipterocarpol, afforded a series of new dammarane triterpenoids containing 2-cyanoethoxy fragment at the carbon atom in the position 3 of the tetracyclic scaffold. A notable antiviral activity was found in 20(S)-3-[(2-cyanoethoxy)imino]-dammar-24-en-20-ol and 20(S)-3-O-(2-cyanoethyl)-25,26,27-trinor-20,24-olidedammarane.

U2 - 10.1134/S1070428015110184

DO - 10.1134/S1070428015110184

M3 - Article

SP - 1627

EP - 1632

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 11

ER -

ID: 3999255