Palladium-catalyzed oxidative alkynylation of arene C-H bond using the chelation-assisted strategy

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Palladium-catalyzed alkynylation of arene C-H bonds with (triisopropylsilyl)acetylene was developed for the first time under oxidative conditions in the present study. Among various type of directing groups examined, the N-phenyl-2-aminopyridine skeleton was shown to be most effective and selective for the Pd-catalyzed direct alkynylation reaction, and the desired alkynylated products were obtained in moderate to good yields. (C) 2012 Elsevier Ltd. All rights reserved.
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Issue Date
2012-07
Language
English
Article Type
Article
Keywords

CARBOXYLIC-ACID DERIVATIVES; CARBON-HYDROGEN BONDS; METAL-FREE CONDITIONS; TERMINAL ALKYNES; ACETYLENE DERIVATIVES; SONOGASHIRA REACTION; DIRECT ARYLATION; DIRECT AMINATION; ARYL; FUNCTIONALIZATION

Citation

TETRAHEDRON, v.68, no.26, pp.5162 - 5166

ISSN
0040-4020
DOI
10.1016/j.tet.2012.04.003
URI
http://hdl.handle.net/10203/101861
Appears in Collection
CH-Journal Papers(저널논문)
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