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.: Synthesis of Arylated Benzofurans by Regioselective Suzuki-Miyaura Cross-Coupling Reactions of 2,3-Dibromobenzofurans- and 2,3,5-Tribromobenzofurans.
J. Heterocycl. Chem. 52 (2), 497-505, 2015.

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Q4 Organic Chemistry

title:

Synthesis of Arylated Benzofurans by Regioselective Suzuki-Miyaura Cross-Coupling Reactions of 2,3-Dibromobenzofurans- and 2,3,5-Tribromobenzofurans

authors:

Hussain, M.
Thai Hung, N.
Abbas, N.
Khera, Rasheed Ahmad
Malik, Imran
Patonay Tamás
Kelzhanova, N.
Abilov, Z. A.
Villinger, Alexander
Langer, Peter

published:

2015

type:

article

genre:

research article/review article

journal:

Journal Of Heterocyclic Chemistry (ISSN: 0022-152X)

language:

English

HAC:

Natural Sciences, Chemical Sciences

subjects:

Molekulatudomány

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.

projects:

TÁMOP-4.2.1/B-09/1/KONV-2010-0007