New Approach to 1,4-Benzoxazin-3-ones by Electrochemical C?H Amination
1,4-Benzoxazin-3-ones are important structural motifs in natural products and bioactive compounds. Usually, the synthesis of benzoxazinones requires transition-metal catalysts and pre-functionalized substrates such as aryl halides. However, the anodic C?H
Wesenberg, Lars Julian,Herold, Sebastian,Shimizu, Akihiro,Yoshida, Jun-Ichi,Waldvogel, Siegfried R.
supporting information
p. 12096 - 12099
(2017/09/13)
An efficient cascade synthesis of various 2H-1,4-benzoxazin-3-(4H)-ones from o-halophenols and 2-halo-amides catalyzed by CuI
A novel and efficient one-pot cascade synthesis of 2H-1,4-benzoxazin-3-(4H) -ones has been developed through copper-catalyzed coupling of o-halophenols and 2-halo-amides. Various 2H-1,4-benzoxazin-3-(4H)-ones with diversity at three substituents on their
Chen, Dingben,Shen, Guodong,Bao, Weiliang
experimental part
p. 4067 - 4073
(2009/12/05)
Anti-inflammatory properties of a series of phenyl- and phenoxy-alkanoic acids.
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Drain,Daly,Davy,Horlington,Howes,Scruton,Selway
p. 684 - 693
(2007/10/08)
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