132120-37-7Relevant articles and documents
Metal-Free Diaryl Etherification of Tertiary Amines by Ortho-C(sp2)-H Functionalization for Synthesis of Dibenzoxazepines and -ones
Jamsheena, Vellekkatt,Mahesha, Chikkagundagal K.,Joy, M. Nibin,Lankalapalli, Ravi S.
supporting information, p. 6614 - 6617 (2017/12/26)
A phenyliodine(III) diacetate mediated umpolung reactivity of the tertiary amines with suitably substituted o-hydroxybenzyl and phenyl groups is exploited to facilitate o-C(sp2)-H functionalization to afford diaryl ethers. The presence of an o-
Synthesis of new benzoxazaphosphinine/benzoxazaphosphole/ diazaphosphaphenalene-2-sulfides using Lawesson's reagent
Prasad, G. Syam,Babu, B. Hari,Reddy, C. Devendranath,Raju, C. Naga,Reddy, C. Suresh
, p. 85 - 91 (2008/03/14)
Synthesis of new benzoxazaphosphinine/benzoxazaphosphole/ diazaphosphaphenalene 2-sulfides were accomplished by the reaction of Lawesson's reagent (LR) with 4-bromo-2-[(phenylamino) methyl]phenol (1a), 4-bromo-2-[(4-chloro/bromo/methoxy/methylphenyl-amino)methyl]phenol (1b-e), 4-bromo-2-[(benzylamino)methyl]phenol (1f), 2-amino-4-chlorophenol (2a)/2-amino-4-methylphenol (2b), 1,8-diaminonaphthalene (3) respectively in anhydrous toluene. Products 4a-f, 5a-b and 6 were characterized by IR, 1H, 13C, 31P NMR and Mass spectra. Copyright Taylor & Francis Group, LLC.