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Citation
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HERO ID
6975836
Reference Type
Journal Article
Title
Syntheses of Novel Tetrasubstituted Thiophenes from Benzene-1,2-Diamines, Ethyl Bromopyruvate, Malononitrile, and Aryl Isothiocyanates
Author(s)
Piltan, M; ,
Year
2020
Is Peer Reviewed?
1
Journal
Polycyclic Aromatic Compounds
ISSN:
1040-6638
EISSN:
1563-5333
Publisher
TAYLOR & FRANCIS LTD
Location
ABINGDON
Volume
41
Issue
10
Page Numbers
2103-2109
DOI
10.1080/10406638.2019.1710854
Web of Science Id
WOS:000506543000001
URL
https://www.proquest.com/docview/2597363080?accountid=171501&bdid=64580&_bd=81qHO9EQxitjEDKzJ%2BR4NE3BHDg%3D
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Abstract
Synthesis of highly functionalized tetrasubstituted thiophenes has been reported involving 3-(bromomethyl)quinoxalin-2(1H)-ones as activated halomethylene compounds precursors. Thus sequential base mediated condensation of readily available malononitrile with aryl isothiocyanates followed by S-alkylation of the resulting enethiolate salts with 3-(bromomethyl)quinoxalin-2(1H)-one compounds and concurrent intramolecular enamine type condensation of S-alkylated compounds affords substituted thiophenes in excellent yields.
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