106782-22-3Relevant articles and documents
Multicomponent synthesis of dihydrobenzoxazepinones by coupling Ugi and Mitsunobu reactions
Banfi, Luca,Guanti, Giuseppe,Basso, Andrea,Lecinska, Paulina,Riva, Renata
, p. 4236 - 4240 (2008/09/18)
Various dihydrobenzo[f][1,4]oxazepin-5-ones have been convergently prepared in 2-3 steps by coupling Ugi and Mitsunobu reactions. Two alternative methodologies were used: in the first one the Ugi condensation was followed by a Mitsunobu cyclization (2 ste
HYDROGENATION OF 3,4-PYRIDYLIDENE AMINOETHANOLS AND FLOTATION PROPERTIES OF THE PRODUCTS OF THEIR REDUCTION
Kukharev, B. F.,Stankevich, V. K.,Klimenko, G. R.,Bel'kova, O. N.
, p. 1307 - 1309 (2007/10/02)
2-(Pyridylmethylene amino)ethanols A-(HOCH2CH2CH2N=CH)C5H4N were obtained by condensation of 3- and 4-pyridinealdehydes with monoethanolamine.IR and PMR spectra are quoted for the substances obtained, as well as data on their application in flotation of lead-zinc ore.By hydrogenation on Raney nickel at 65 deg C and 70 atm hydrogen pressure 2-(pyridylmethyl amino) ethanols A-(HOCH2CH2NHCH2)C5H4N were obtained.