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N-Arylations of sulfoximines with 2-arylpyridines by copper-mediated dual N-H/C-H activation

Version 2 2024-06-13, 10:23
Version 1 2014-05-01, 00:00
journal contribution
posted on 2024-06-13, 10:23 authored by L Wang, DL Priebbenow, W Dong, C Bolm
A high-yielding method providing rapid access to new N-arylated sulfoximines has been developed. A stoichiometric amount of copper facilitates the C-H activation of 2-arylpyridines which then undergo oxidative C-N cross-couplings with various sulfoximine derivatives.

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Location

Washington, United States

Language

eng

Publication classification

C Journal article, C1.1 Refereed article in a scholarly journal

Copyright notice

2014 American Chemical Society

Journal

Organic letters

Volume

16

Pagination

2661-2663

ISSN

1523-7060

eISSN

1523-7052

Issue

10

Publisher

American Chemical Society

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