In:
Angewandte Chemie, Wiley, Vol. 129, No. 18 ( 2017-04-24), p. 5207-5211
Abstract:
Meta‐C−H functionalization of benzylamines has been developed using a Pd II /transient mediator strategy. Using 2‐pyridone ligands and 2‐carbomethoxynorbornene (NBE‐CO 2 Me) as the mediator, arylation, amination, and chlorination of benzylamines are realized. This protocol features a broad substrate scope and is compatible with heterocylic coupling partners. Moreover, the loading of the Pd can be lowered to 2.5 mol % by using the optimal ligand.
Type of Medium:
Online Resource
ISSN:
0044-8249
,
1521-3757
DOI:
10.1002/ange.v129.18
DOI:
10.1002/ange.201701803
Language:
English
Publisher:
Wiley
Publication Date:
2017
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