Synthesis of aurone derivatives on the basis of 2,4,6-trihydroxytoluene Full article
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Chemistry of Heterocyclic Compounds
ISSN: 1573-8353 , E-ISSN: 0009-3122 |
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| Output data | Year: 2019, Volume: 55, Number: 12, Pages: 1174-1178 Pages count : 5 DOI: 10.1007/s10593-019-02597-0 | ||||
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Abstract:
2,4,6-Trihydroxytoluene (2-methylphloroglucinol) was used as starting material for the first synthesis of several (Z)-2-arylidene-4,6-dihydroxy-7-methylaurones, including a synthetic analog of the natural 7-methylaureusidin, which is currently obtained mainly from the extract of sedge capitata (Cyperus capitatus). It was shown that the reaction of 2,4,6-trihydroxytoluene with chloroacetonitrile occurred regioselectively, with the formation of 4,6-dihydroxy-7-methylbenzofuran-3(2H)-one, the treatment of which with substituted benzaldehydes gave high yields of the target compounds.
Cite:
Shubin D.A.
, Kuznetsov D.N.
, Kobrakov K.I.
, Starosotnikov A.M.
, Merkulova N.L.
Synthesis of aurone derivatives on the basis of 2,4,6-trihydroxytoluene
Chemistry of Heterocyclic Compounds. 2019. V.55. N12. P.1174-1178. DOI: 10.1007/s10593-019-02597-0 WOS Scopus OpenAlex
Synthesis of aurone derivatives on the basis of 2,4,6-trihydroxytoluene
Chemistry of Heterocyclic Compounds. 2019. V.55. N12. P.1174-1178. DOI: 10.1007/s10593-019-02597-0 WOS Scopus OpenAlex
Identifiers:
| Web of science: | WOS:000504155300002 |
| Scopus: | 2-s2.0-85077164726 |
| OpenAlex: | W2996491544 |