Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/23364
Title: [Cp*RhCl2]2-catalyzed ortho-C-H bond amination of acetophenone o-methyloximes with primary N-chloroalkylamines : convenient synthesis of N-alkyl-2-acylanilines
Authors: Ng, KH
Zhou, Z
Yu, WY 
Issue Date: 2013
Publisher: Royal Society of Chemistry
Source: Chemical communications, 2013, v. 49, no. 63, p. 7031-7033 How to cite?
Journal: Chemical communications 
Abstract: Rh(iii)-catalyzed aromatic C-H amination of acetophenone o-methyloximes with primary N-chloroalkylamines was developed, and the arylamine products were obtained in up to 92% yield. The reaction probably involves rate-limiting electrophilic C-H bond cleavage (kH/kD = 2).
URI: http://hdl.handle.net/10397/23364
ISSN: 1359-7345
EISSN: 1364-548X
DOI: 10.1039/c3cc42937g
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