1349866-01-8Relevant articles and documents
The reported formation of 5H-dibenzo[b,e][1,4]diazepin-11(10H)-ones in the noncatalyzed, base-promoted double arylation of anthranilamide revisited. Correction of some product structures
Wróbel, Zbigniew,Wilk, Bogdan,Cmoch, Piotr,Kwast, Andrzej
, p. 1802 - 1808 (2021)
The base-promoted reaction of 2-halonitro- or 1,2-dihalobenzenes with anthranilamide reported by Cao, Ma et al. (Synthesis 2013, 45, 111) was reinvestigated. Some of the products reported, which have been identified as dibenzodiazepinones, are actually be
Nickel-catalyzed decarboxylative arylation of heteroarenes through sp2 C-H functionalization
Yang, Ke,Wang, Peng,Zhang, Cheng,Kadi, Adnan A.,Fun, Hoong-Kun,Zhang, Yan,Lu, Hongjian
supporting information, p. 7586 - 7589 (2015/04/22)
The direct decarboxylative arylation of hetereoarenes with benzoic acids through a nickel-catalyzed sp2 C-H functionalization process was developed. This process provides the first examples of decarboxylative cross-coupling reactions with aroma