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Back Cover: Monoprotected l ‐Amino Acid ( l ‐MPAA), Accelerated Bromination, Chlorination, and Iodination of C(sp 2 )−H Bonds by Iridium(III) Catalysis (Chem. Eur. J. 29/2017)
Author(s) -
Kathiravan Subban,
Nicholls Ian A.
Publication year - 2017
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201701074
Subject(s) - halogenation , iridium , chemistry , catalysis , derivative (finance) , medicinal chemistry , stereochemistry , organic chemistry , financial economics , economics
Mono‐protected l ‐amino acid ( l ‐MPAA) ‐accelerated iridium(III)‐catalyzed halogenation of (hetero)anilides at room temperature provides a general route to halogenation (Cl, Br, I) of (hetero)arenes through C(sp 2 )−H activation. The synthetic utility of the method was demonstrated through the synthesis of a quinolone derivative. More information can be found in the Full Paper by I. A. Nicholls and S. Kathiravan on page 7031.

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