Highly efficient iodine-catalyzed hydroarylation of arenes with styrenes

Iodine mediates the hydroarylation of styrenes with arenes and heteroarenes to afford 1,1-diarylalkanes in good to high yields. Details regarding the substrate scope and selectivity of this hydroarylation reaction are discussed.

Saved in:
Bibliographic Details
Published inTetrahedron letters Vol. 48; no. 39; pp. 6881 - 6885
Main Authors Chu, Cheng-Ming, Huang, Wan-Ju, Liu, Ju-Tsung, Yao, Ching-Fa
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 24.09.2007
Elsevier
Subjects
Chemistry
Chemistry, Organic
Friedel–Crafts reaction
Heteroarenes
Hydroarylation
Iodine
Physical Sciences
Science & Technology
Styrene
Hydroarylation
Friedel–Crafts reaction
Heteroarenes
Styrene
Iodine
MOLECULAR-IODINE
3-COMPONENT SYNTHESIS
ONE-POT SYNTHESIS
AROMATIC IMINES
CARBON-HYDROGEN BONDS
H BOND FUNCTIONALIZATION
heteroarenes
RETRACTED ARTICLE. SEE
iodine
hydroarylation
FRIEDEL-CRAFTS ALKYLATION
ELECTRON-RICH ARENES
Friedel-Crafts reaction
styrene
CONJUGATE ADDITION
Online AccessGet full text

Cover

More Information
Summary:Iodine mediates the hydroarylation of styrenes with arenes and heteroarenes to afford 1,1-diarylalkanes in good to high yields. Details regarding the substrate scope and selectivity of this hydroarylation reaction are discussed.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2007.07.178