Pd-Catalyzed one-pot sequential cross-coupling reactions of tetrabromothiophene
Author:
Affiliation:
1. Synthetic Organic Chemistry Research Laboratory
2. Department of Chemistry
3. University of Delhi
4. Delhi
5. India
Abstract
Unsymmetrical one-pot sequential cross-coupling reactions of sterically hindered tetrabromothiophene with arylboronic acid and an alkyne/alkene to afford selective bi-, tri-, and tetrasubstituted aryl/alkynyl-thiophenes with the aid of a palladium catalyst were described.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB02601C
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