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

Yurii V. Kharitonov; Makhmut M. Shakirov; Elvira E. Shults

doi:10.6060/mhc160959s

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

Yurii V. Kharitonov, Makhmut M. Shakirov, Elvira E. Shults

Лаборатория радиоуглеродных методов анализа ФФ

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

1 Цитирования (Scopus)

Аннотация

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.

Язык оригинала	английский
Страницы (с-по)	117-122
Число страниц	6
Журнал	Macroheterocycles
Том	10
Номер выпуска	1
DOI	https://doi.org/10.6060/mhc160959s
Состояние	Опубликовано - 1 янв 2017

Доступ к документу

10.6060/mhc160959s

Link to publication in Scopus

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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",

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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.

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

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