Synthesis of functionalized imidazo[4,5-e]thiazolo[3,2-b]triazines by condensation of imidazo[4,5-e]triazinethiones with DMAD or DEAD and rearrangement to imidazo[4,5-e]thiazolo[2,3-c]triazines Full article
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Beilstein Journal of Organic Chemistry
ISSN: 2195-951X , E-ISSN: 1860-5397 |
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| Output data | Year: 2021, Volume: 17, Pages: 1141-1148 Pages count : 8 DOI: 10.3762/bjoc.17.87 | ||||||
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Abstract:
Two series of functionalized imidazothiazolotriazine derivatives were synthesized via the condensation of imidazo[4,5-e]-1,2,4-triazine-3-thiones with acetylenedicarboxylic acid dimethyl and diethyl esters (DMAD and DEAD) and subsequent base-catalyzed rearrangement of the obtained imidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazines into regioisomeric imidazo[4,5-e]thiazolo[2,3-c]-1,2,4-triazine derivatives.
Cite:
Izmest’ev A.N.
, Vinogradov D.B.
, Kolotyrkina N.G.
, Kravchenko A.N.
, Gazieva G.A.
Synthesis of functionalized imidazo[4,5-e]thiazolo[3,2-b]triazines by condensation of imidazo[4,5-e]triazinethiones with DMAD or DEAD and rearrangement to imidazo[4,5-e]thiazolo[2,3-c]triazines
Beilstein Journal of Organic Chemistry. 2021. V.17. P.1141-1148. DOI: 10.3762/bjoc.17.87 WOS Scopus OpenAlex
Synthesis of functionalized imidazo[4,5-e]thiazolo[3,2-b]triazines by condensation of imidazo[4,5-e]triazinethiones with DMAD or DEAD and rearrangement to imidazo[4,5-e]thiazolo[2,3-c]triazines
Beilstein Journal of Organic Chemistry. 2021. V.17. P.1141-1148. DOI: 10.3762/bjoc.17.87 WOS Scopus OpenAlex
Identifiers:
| ≡ Web of science: | WOS:000651414700001 |
| ≡ Scopus: | 2-s2.0-85106371088 |
| ≡ OpenAlex: | W3163113771 |