Journal
TETRAHEDRON LETTERS
Volume 51, Issue 18, Pages 2420-2422Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2010.02.141
Keywords
Catalysis; Palladium; Suzuki-Miyaura reaction; Site-selectivity; Benzofuran
Categories
Funding
- State of Pakistan (HEC)
- DAAD
- State of Vietnam (MOET)
- State of Mecklenburg-Vorpommern
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The Suzuki-Miyaura reaction of 2,3-dibromobenzofuran with two equivalents of boronic acids gave 2,3-diarylbenzofurans. The reaction with one equivalent of arylboronic acids resulted in site-selective formation of 2-aryl-3-bromobenzofurans. 2,3-Diarylbenzofurans containing two different aryl groups were prepared from 2,3-dibromobenzofuran in a one-pot protocol by sequential addition of two different boronic acids. (C) 2010 Elsevier Ltd. All rights reserved.
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