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Direct synthesis of anthracenes from o-tolualdehydes and aryl iodides through Pd(II)-Catalyzed sp3 CH arylation and electrophilic aromatic cyclization
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Title
Direct synthesis of anthracenes from o-tolualdehydes and aryl iodides through Pd(II)-Catalyzed sp3 CH arylation and electrophilic aromatic cyclization
Issued Date
2018-04
Citation
Park, H. (2018-04). Direct synthesis of anthracenes from o-tolualdehydes and aryl iodides through Pd(II)-Catalyzed sp3 CH arylation and electrophilic aromatic cyclization. Tetrahedron, 74(16), 2048–2055. doi: 10.1016/j.tet.2018.03.006
Type
Article
Author Keywords
Transient directing groupsC-H activationsp(3) C-H arylationOne-pot synthesisAnthracenes
Keywords
METAL-ORGANIC FRAMEWORKBOND ACTIVATIONATOM ECONOMYC(SP(3))-H ARYLATIONALIPHATIC-KETONESNATURAL-PRODUCTSFUNCTIONALIZATIONCONSTRUCTIONDERIVATIVESCATALYSIS
ISSN
0040-4020
Abstract
The first direct synthesis of substituted anthracenes from o-tolualdehydes and aryl iodides via a Pd(II)-catalyzed C. H arylation using an alcohol-bearing transient directing group and subsequent AgOTf-assisted electrophilic aromatic cyclization is described. New transient directing groups consisting of amino acids and amino alcohols enhanced the reactivity, and the C. H arylation was complete in 12 h at 90 °C. By simply changing the silver salt to silver triflate, the one-pot synthesis of anthracene derivatives was carried out using the present reaction conditions. © 2018 Elsevier Ltd.
URI
http://hdl.handle.net/20.500.11750/6142
DOI
10.1016/j.tet.2018.03.006
Publisher
Elsevier Ltd
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정병혁
Jung, Byunghyuck정병혁

Department of Physics and Chemistry

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