Chemoselective: N -arylation of aminobenzamides via copper catalysed Chan-Evans-Lam reactions
Chemoselective N-arylation of unprotected aminobenzamides was achieved via Cu-catalysed Chan-Evans-Lam cross-coupling with aryl boronic acids for the first time. Simple copper catalysts enable the selective arylation of amino groups in ortho/meta/para-aminobenzamides under open-flask conditions. The reactions were scalable and compatible with a wide range of functional groups.
Liu, Shuai,Zu, Weisai,Zhang, Jinli,Xu, Liang
p. 9288 - 9292
(2017/11/23)
Studies on 4(1H)-quinazolinones. I. A convenient synthesis and some reactions of 1-phenyl-2-substituted-4(1H)-quinazolinones
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Ozaki,Yamada,Oine
p. 702 - 707
(2007/10/02)
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