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A Simple Synthesis of Angular Anthrathiophenediones via Acetylenic Derivatives of Anthraquinone Full article

Journal Synthesis (Synthesis-Stuttgart)
ISSN: 0039-7881 , E-ISSN: 1437-210X
Output data Year: 2004, Number: 13, Pages: 2131-2134 Pages count : 4 DOI: 10.1055/s-2004-829187
Tags Alkynes, Cross-coupling, Quinones, Ring closure, Sulfur
Authors Ivanchikova Irena D. , Lebedeva Nadezhda I. , Shvartsberg Mark S.
Affiliations
1 Institute of Chemical Kinetics and Combustion, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090, Russia

Abstract: Condensation of 2-alkynyl-1-chloro- and 1-alkynyl-2-chloroanthraquinones with Na2S under mild conditions afforded anthra[1,2-b]thiophene-6,11-diones and anthra[2,1-b]thiophene-6,11-diones, respectively. A variety of angular anthrathiophenediones was synthesized by this method. The acetylenic precursors were prepared by a modified procedure of the Sonogashira reaction.
Cite: Ivanchikova I.D. , Lebedeva N.I. , Shvartsberg M.S.
A Simple Synthesis of Angular Anthrathiophenediones via Acetylenic Derivatives of Anthraquinone
Synthesis (Synthesis-Stuttgart). 2004. N13. P.2131-2134. DOI: 10.1055/s-2004-829187 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Feb 24, 2004
Accepted: May 24, 2004
Published print: Sep 6, 2004
Identifiers:
Web of science: WOS:000223845000009
Scopus: 2-s2.0-4544364091
Elibrary: 13473407
Chemical Abstracts: 2004:767859
Chemical Abstracts (print): 141:395365
OpenAlex: W2949566931
Citing:
DB Citing
Web of science 21
Scopus 24
OpenAlex 7
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