1640100-48-6Relevant articles and documents
TBHP/R4N+X– promoted hydroaroylation of dialkyl azodicarboxylates with methyl arenes, aldehydes, aryl methanols and arylmethyl chlorides
Adib, Mehdi,Pashazadeh, Rahim,Rajai-Daryasarei, Saideh,Moradkhani, Fatemeh,Jahani, Mehdi,Gohari, Seyed Jamal Addin
, p. 3858 - 3870 (2018)
Efficient TBHP/R4N+X– promoted hydroaroylations of dialkyl azo-1,2-dicarboxylates with methyl arenes, aldehydes, aryl methanols and arylmethyl chlorides are described. These oxidation/oxygenation and hydroaroylation processes were carried out by tert-butyl hydroperoxide as terminal oxidant/oxygen source, and were catalyzed by tetrabutylammonium bromide and tricaprylmethylammonium chloride as the driving force. During this investigation, all these hydroaroylating sources were found to be highly efficient reagents without the need of any transition-metal.
Lewis- and Bronsted-acid cooperative catalytic radical coupling of aldehydes and azodicarboxylate
Zhang, Hong-Bo,Wang, Yao,Gu, Yun,Xu, Peng-Fei
, p. 27796 - 27799 (2014/07/21)
An efficient radical coupling reaction of aldehydes and azodicarboxylate was developed by using the strategy of merging Lewis- and Bronsted- acid catalysis. This journal is the Partner Organisations 2014.