期刊
TETRAHEDRON LETTERS
卷 51, 期 21, 页码 2810-2812出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2010.03.067
关键词
Catalysis; Suzuki-Miyaura reaction; Site-selectivity; Palladium; Organofluorine compounds
资金
- DAAD
- University of Rostock
The Suzuki-Miyaura reaction of 1,4-dibromo-2-fluorobenzene with two equivalents of arylboronic acids gave fluorinated paro-terphenyls. The reaction with 1 equiv of arylboronic acid resulted in site-selective formation of biphenyls. The one-pot reaction of 1,4-dibromo-2-fluorobenzene with two different arylboronic acids afforded fluorinated para-terphenyls containing two different terminal aryl groups. (C) 2010 Elsevier Ltd. All rights reserved.
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