Synthesis of Macroheterocyclic Compounds with a Furan Bridge Possessing Structural Fragments of 1,2,3-Triazoles and Natural Diterpenoids

Synthesis of Macroheterocyclic Compounds with a Furan Bridge Possessing Structural Fragments of 1,2,3-Triazoles and Natural Diterpenoids Full article

Journal

Macroheterocycles
ISSN: 1998-9539

Output data

Year: 2015, Volume: 8, Number: 1, Pages: 81-88 Pages count : DOI: 10.6060/mhc141138s

Tags

Lambertianic acid; labdanoid alkynes; azides; click chemistry; macroheterocycles

Authors

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

Affiliations

1	(Данные Web of science) Novosibirsk Organ Chem Inst, Novosibirsk 630090, Russia
2	(Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia

Derivatives of natural diterpenoid lambertianic acid containing alkyne and dialkyne substituent in the furan ring were obtained. 1,2,3-Triazole-incarporated furan bridged macrocycles have been prepared by 1,3-dipolar cycloaddition of methyl 15,16-bis[(prop-2-yn-1-yloxy)methyl] lambertianate with various diazides in the presence of Cu(II)/sodium ascorbate in methylene chloride/water reaction medium.

Kharitonov Y.V. , Shakirov M.M. , Shults E.E.
Synthesis of Macroheterocyclic Compounds with a Furan Bridge Possessing Structural Fragments of 1,2,3-Triazoles and Natural Diterpenoids

Macroheterocycles. 2015. V.8. N1. P.81-88. DOI: 10.6060/mhc141138s WOS Scopus РИНЦ

Full text from publisher

Web of science	WOS:000358530500011
Scopus	2-s2.0-84932649180
Elibrary	23757219
OpenAlex	W2553948439