Synthesis of Novel Labdanoid-Based Macroheterocycles Using Click-Cycloaddition Reaction Protocol

Synthesis of Novel Labdanoid-Based Macroheterocycles Using Click-Cycloaddition Reaction Protocol Научная публикация

Журнал

Macroheterocycles
ISSN: 1998-9539

Вых. Данные

Год: 2017, Том: 10, Номер: 1, Страницы: 117-122 Страниц : 6 DOI: 10.6060/mhc160959s

Ключевые слова

Diterpenoids; lamberianic acid; dialkynes; diazides; CuAAC-reaction; macrocycles

Авторы

Kharitonov Yurii V. ^1,2 , Shakirov Makhmut M. ¹ , Shults Elvira E. ^1,2

Организации

1	(Данные Web of science) Russian Acad Sci, Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia
2	(Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia

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.

Kharitonov Y.V. , Shakirov M.M. , Shults E.E.
Synthesis of Novel Labdanoid-Based Macroheterocycles Using Click-Cycloaddition Reaction Protocol

Macroheterocycles. 2017. V.10. N1. P.117-122. DOI: 10.6060/mhc160959s WOS Scopus РИНЦ

Полный текст от издателя

Web of science	WOS:000405134200017
Scopus	2-s2.0-85052806490
РИНЦ	29332741
OpenAlex	W2622336686