Standard

Synthesis of novel labdanoid–Based macroheterocycles using click–Cycloaddition reaction protocol. / Kharitonov, Yurii V.; Shakirov, Makhmut M.; Shults, Elvira E.

в: Macroheterocycles, Том 10, № 1, 01.01.2017, стр. 117-122.

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

Harvard

Kharitonov, YV, Shakirov, MM & Shults, EE 2017, 'Synthesis of novel labdanoid–Based macroheterocycles using click–Cycloaddition reaction protocol', Macroheterocycles, Том. 10, № 1, стр. 117-122. https://doi.org/10.6060/mhc160959s

APA

Kharitonov, Y. V., Shakirov, M. M., & Shults, E. E. (2017). Synthesis of novel labdanoid–Based macroheterocycles using click–Cycloaddition reaction protocol. Macroheterocycles, 10(1), 117-122. https://doi.org/10.6060/mhc160959s

Vancouver

Kharitonov YV, Shakirov MM, Shults EE. Synthesis of novel labdanoid–Based macroheterocycles using click–Cycloaddition reaction protocol. Macroheterocycles. 2017 янв. 1;10(1):117-122. doi: 10.6060/mhc160959s

Author

Kharitonov, Yurii V. ; Shakirov, Makhmut M. ; Shults, Elvira E. / Synthesis of novel labdanoid–Based macroheterocycles using click–Cycloaddition reaction protocol. в: Macroheterocycles. 2017 ; Том 10, № 1. стр. 117-122.

BibTeX

@article{ad18f197f1184b10be50b347efbe01be,
title = "Synthesis of novel labdanoid–Based macroheterocycles using click–Cycloaddition reaction protocol",
abstract = "A convenient synthetic method to diterpenoid dialkyne 18-propargyloxy-16-[(prop-2-yn-1-yloxi)methyl]labda-8(17),13,15-triene in the common yield of 34% from the natural plant diterpenoid lambertianic acid was developed. 1,2,3-Triazolyl containing macroheterocyclic compounds with an integrated diterpenoid fragment have been prepared by CuAAC reaction of the labdanoid dialkyne with organic diazides.",
keywords = "CuAAC-reaction, Dialkynes, Diazides, Diterpenoids, Lamberianic acid, Macrocycles",
author = "Kharitonov, {Yurii V.} and Shakirov, {Makhmut M.} and Shults, {Elvira E.}",
year = "2017",
month = jan,
day = "1",
doi = "10.6060/mhc160959s",
language = "English",
volume = "10",
pages = "117--122",
journal = "Macroheterocycles",
issn = "1998-9539",
publisher = "Ivanovo State University of Chemistry and Technology",
number = "1",

}

RIS

TY - JOUR

T1 - Synthesis of novel labdanoid–Based macroheterocycles using click–Cycloaddition reaction protocol

AU - Kharitonov, Yurii V.

AU - Shakirov, Makhmut M.

AU - Shults, Elvira E.

PY - 2017/1/1

Y1 - 2017/1/1

N2 - A convenient synthetic method to diterpenoid dialkyne 18-propargyloxy-16-[(prop-2-yn-1-yloxi)methyl]labda-8(17),13,15-triene in the common yield of 34% from the natural plant diterpenoid lambertianic acid was developed. 1,2,3-Triazolyl containing macroheterocyclic compounds with an integrated diterpenoid fragment have been prepared by CuAAC reaction of the labdanoid dialkyne with organic diazides.

AB - A convenient synthetic method to diterpenoid dialkyne 18-propargyloxy-16-[(prop-2-yn-1-yloxi)methyl]labda-8(17),13,15-triene in the common yield of 34% from the natural plant diterpenoid lambertianic acid was developed. 1,2,3-Triazolyl containing macroheterocyclic compounds with an integrated diterpenoid fragment have been prepared by CuAAC reaction of the labdanoid dialkyne with organic diazides.

KW - CuAAC-reaction

KW - Dialkynes

KW - Diazides

KW - Diterpenoids

KW - Lamberianic acid

KW - Macrocycles

UR - http://www.scopus.com/inward/record.url?scp=85052806490&partnerID=8YFLogxK

U2 - 10.6060/mhc160959s

DO - 10.6060/mhc160959s

M3 - Article

AN - SCOPUS:85052806490

VL - 10

SP - 117

EP - 122

JO - Macroheterocycles

JF - Macroheterocycles

SN - 1998-9539

IS - 1

ER -

ID: 16410094