SYNTHESIS OF ANGULAR HETEROCYCLIC-DERIVATIVES OF ANTHRAQUINONE BY INTRAMOLECULAR CYCLIZATION Full article
Journal |
SIBIRSKII KHIMICHESKII ZHURNAL
ISSN: 0134-2428 |
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Output data | Year: 1992, Number: 4, Pages: 52-57 Pages count : |
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Abstract:
For the synthesis of angular heterocyclic anthraquinone derivatives intramolecular cyclization reactions of monosubstituted anthraquinones are very attractive (from practical viewpoint) reactions proceeding by the mechanism of direct hydrogen substitution in the benzoid ring. The review deals with known examples of intramolecular alkylation, arylation, acylation, amination and thiylation of alpha-substituted anthraquinones with forming of angular five- and six-membered heterocycles containing nitrogen, sulfur and oxygen atoms.
Cite:
Saveliev V.A.
, Loskutov V.A.
SYNTHESIS OF ANGULAR HETEROCYCLIC-DERIVATIVES OF ANTHRAQUINONE BY INTRAMOLECULAR CYCLIZATION
SIBIRSKII KHIMICHESKII ZHURNAL. 1992. N4. P.52-57. WOS
SYNTHESIS OF ANGULAR HETEROCYCLIC-DERIVATIVES OF ANTHRAQUINONE BY INTRAMOLECULAR CYCLIZATION
SIBIRSKII KHIMICHESKII ZHURNAL. 1992. N4. P.52-57. WOS
Identifiers:
Web of science | WOS:A1992KK37900007 |