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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

Abstract: 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.
Cite: 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 OpenAlex
Files: Full text from publisher
Identifiers:
Web of science: WOS:000358530500011
Scopus: 2-s2.0-84932649180
Elibrary: 23757219
OpenAlex: W2553948439
Citing:
DB Citing
Web of science 5
Scopus 6
Elibrary 7
OpenAlex 2
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