Ionic liquid-mediated synthesis of (1H-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes

Ionic liquid-mediated synthesis of (1H-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes Full article

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2015, Volume: 25, Number: 4, Pages: 257-259 Pages count : 3 DOI: 10.1016/j.mencom.2015.07.007

Authors

Fershtat Leonid L. ¹ , Ashirbaev Salavat S. ¹ , Kulikov Alexander S. ¹ , Kachala Vadim V. ¹ , Makhova Nina N. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

The [3 + 2] cycloaddition of azidofuroxans to internal and terminal acetylenes was found to occur only in ionic liquids on heating and afford (1H-1,2,3-triazol-1-yl)furoxans in moderate to good yields. The reaction with terminal acetylenes proceeds with high regio- selectivity.

Fershtat L.L. , Ashirbaev S.S. , Kulikov A.S. , Kachala V.V. , Makhova N.N.
Ionic liquid-mediated synthesis of (1H-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes
Mendeleev Communications. 2015. V.25. N4. P.257-259. DOI: 10.1016/j.mencom.2015.07.007 WOS Scopus OpenAlex

≡ Web of science:	WOS:000360416600007
≡ Scopus:	2-s2.0-84938698034
≡ OpenAlex:	W2265167145