92755-81-2Relevant articles and documents
Stereospecific 1,3-Aminobromination of Donor–Acceptor Cyclopropanes
Das, Saikat,Daniliuc, Constantin G.,Studer, Armido
supporting information, p. 11554 - 11558 (2017/09/11)
Sn(OTf)2-catalyzed 1,3-aminobromination of donor–acceptor cyclopropanes with various sulfonyl amides or electron-poor anilines and N-bromosuccinimide is reported. These experimentally straightforward reactions occurred with complete regio- and
Au(iii)-catalyzed intermolecular amidation of benzylic C-H bonds
Zhang, Yan,Feng, Bainian,Zhu, Chengjian
, p. 9137 - 9141,5 (2012/12/12)
Au(iii)-catalyzed intermolecular amidations of benzylic C-H bonds with sulfonamides and carboxamides are described. The protocol with the Au-bipy complex/N-bromosuccinimide system provides practical applications for synthesis of various amides via C-H activations. The reaction proceeds with high efficiency to give the corresponding amines, which are extremely useful synthetic intermediates.
Palladium(II) mediated aziridination of olefins with bromamine-T as the nitrogen source: scope and mechanism
Antunes, Alexandra M.M.,Bonifácio, Vasco D.B.,Nascimento, Susana C.C.,Lobo, Ana M.,Branco, Paula S.,Prabhakar, Sundaresan
, p. 7009 - 7017 (2008/02/05)
The palladium(II)-promoted reaction of a variety of olefins and bromamine-T provided N-tosyl-2-substituted aziridines under mild conditions. Olefins bearing chiral appendages gave only a poor to modest diastereoselectivity. Appropriate deuterated olefins
