1198-91-0Relevant academic research and scientific papers
Tandem and Selective Conversion of Tetrahydropyranyl and Silyl Ethers to Oximes Catalyzed with Trichloroisocyanuric Acid
Aghapour, Ghasem,Abbaszadeh, Zeinab
, p. 1464 - 1470 (2015/09/01)
Direct and oxidative conversion of tetrahydropyranyl and silyl ethers to oximes is described using trichloroisocyanuric acid (TCCA) as a relatively stable and inexpensive oxidant surprisingly in a catalytic amount and hydroxylamine hydrochloride under solvent-free conditions. Oximes can be synthesized from these protected alcohols in the presence of some other functional groups with excellent chemoselectivity using the present tandem catalytic method.
Europium(III) triflate-catalyzed Trofimov synthesis of polyfunctionalized pyrroles
Madabhushi, Sridhar,Vangipuram, Venkata Sairam,Mallu, Kishore Kumar Reddy,Chinthala, Narsaiah,Beeram, China Ramanaiah
supporting information; body text, p. 1413 - 1416 (2012/07/13)
The synthesis of polyfunctionalized pyrroles by reaction of a ketoxime with dimethyl acetylenedicarboxylate using europium(III) triflate as the catalyst is described. Copyright
LIQUID CHROMATOGRAPHIC RESOLUTION OF RACEMIC KETONES AS THEIR OXIME 3,5-DINITROPHENYL CARBAMATES ON A CHIRAL STATIONARY PHASE
Hyun, Myung Ho,Park, Young -Whan,Baik, In-Kyu
, p. 4735 - 4738 (2007/10/02)
Cyclic and acyclic chiral ketones have been resolved as their oxime 3,5-dinitrophenyl carbamates on a chiral stationary phase derived from (S)-1-(6,7-dimethyl-1-naphthyl)isobutylamine.
C-Nitroso compounds. Part XXXVIII. Radical reactions of α-chloro-nitroso compounds with trialkylaluminium-ether complexes
Lub, J.,Beekes, M. L.,Boer, Th. J. de
, p. 161 - 167 (2007/10/02)
Ether complexes of trialkylaluminium compounds react with α-chloro-nitroso compounds via radicals which can abstract hydrogen from various solvents.In the presence of olefinic solvents, radical addition to the double bond also takes place. When the trialk
