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A Highly Efficient Method for the Copper-Catalyzed Selective Synthesis of Diaryl Chalcogenides from Easily Available Chalcogen Sources

Release Time:2019-03-09  Hits:

Indexed by: Journal Article

Date of Publication: 2011-12-01

Journal: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Included Journals: SCIE、Scopus

Issue: 36

Page Number: 7331-7338

ISSN: 1434-193X

Key Words: Synthetic methods; Selective synthesis; Cross-coupling; Copper; Sulf-ur; Selenium

Abstract: An efficient protocol for copper-catalyzed CS or CSe bond formation between aryl iodides and easily available chalcogen sources leading to diaryl chalcogenides is reported. A variety of symmetrical diaryl sulfides and diaryl selenides were synthesized in good to excellent yields. Unsymmetrical diaryl sulfides were also obtained in moderate yields from two different aryl iodides by a one-pot tandem process. This strategy was further successfully utilized for the synthesis of 2-phenylbenzo[b]thiophene and of [1]benzothieno[3,2-b]benzothiophene.

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