Synthesis of arylated benzofurans by regioselective Suzuki-Miyaura cross-coupling reactions of 2,3-dibromobenzofurans- and 2,3,5-tribromobenzofurans

M. Hussain, N. Thai Hung, N. Abbas, R. A. Khera, I. Malik, T. Patonay, N. Kelzhanova, Z. A. Abilov, A. Villinger, P. Langer

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Arylated benzofurans were prepared by regioselective Suzuki-Miyaura cross-coupling reactions of 2,3-dibromobenzofuran. The reactions proceeded with very good site-selectivity in favor of the more electron deficient position 2. The Suzuki-Miyaura reactions of 2,3,5-tribromobenzofuran also proceeded in favor of position 2.

Original languageEnglish
Pages (from-to)497-505
Number of pages9
JournalJournal of Heterocyclic Chemistry
Volume52
Issue number2
DOIs
Publication statusPublished - 2015

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Benzofurans
Electrons

ASJC Scopus subject areas

  • Organic Chemistry

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Synthesis of arylated benzofurans by regioselective Suzuki-Miyaura cross-coupling reactions of 2,3-dibromobenzofurans- and 2,3,5-tribromobenzofurans. / Hussain, M.; Thai Hung, N.; Abbas, N.; Khera, R. A.; Malik, I.; Patonay, T.; Kelzhanova, N.; Abilov, Z. A.; Villinger, A.; Langer, P.

In: Journal of Heterocyclic Chemistry, Vol. 52, No. 2, 2015, p. 497-505.

Research output: Contribution to journalArticle

Hussain, M. ; Thai Hung, N. ; Abbas, N. ; Khera, R. A. ; Malik, I. ; Patonay, T. ; Kelzhanova, N. ; Abilov, Z. A. ; Villinger, A. ; Langer, P. / Synthesis of arylated benzofurans by regioselective Suzuki-Miyaura cross-coupling reactions of 2,3-dibromobenzofurans- and 2,3,5-tribromobenzofurans. In: Journal of Heterocyclic Chemistry. 2015 ; Vol. 52, No. 2. pp. 497-505.
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AU - Hussain, M.

AU - Thai Hung, N.

AU - Abbas, N.

AU - Khera, R. A.

AU - Malik, I.

AU - Patonay, T.

AU - Kelzhanova, N.

AU - Abilov, Z. A.

AU - Villinger, A.

AU - Langer, P.

PY - 2015

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