A copper(ii) complex as an intermediate of copper(i)-catalyzed C–N cross coupling of N-phenylaniline with aryl halide by in situ ESI-MS study
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Title
A copper(ii) complex as an intermediate of copper(i)-catalyzed C–N cross coupling of N-phenylaniline with aryl halide by in situ ESI-MS study
Authors
Keywords
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Journal
CHEMICAL COMMUNICATIONS
Volume 47, Issue 23, Pages 6686
Publisher
Royal Society of Chemistry (RSC)
Online
2011-05-05
DOI
10.1039/c1cc11906k
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- (2008) Florian Monnier et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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