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Ligand-Controlled, Tunable Silver-Catalyzed C–H Amination
Author(s) -
Juliet M. Alderson,
Alicia M. Phelps,
Ryan J. Scamp,
Nicholas S. Dolan,
Jennifer M. Schomaker
Publication year - 2014
Publication title -
journal of the american chemical society
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja5094309
Subject(s) - nitrene , chemistry , amination , catalysis , ligand (biochemistry) , regioselectivity , combinatorial chemistry , surface modification , organic chemistry , biochemistry , receptor
The development of readily tunable and regioselective C-H functionalization reactions that operate solely through catalyst control remains a challenge in modern organic synthesis. Herein, we report that simple silver catalysts supported by common nitrogenated ligands can be used to tune a nitrene transfer reaction between two different types of C-H bonds. The results reported herein represent the first example of ligand-controlled and site-selective silver-promoted C-H amination.

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