66064-59-3Relevant academic research and scientific papers
1,2-Reduction of α,β-unsaturated hydrazones using dimethylamine-borane/p-toluenesulfonic acid: An easy route to allyl hydrazines
Casarini, Maria E,Ghelfi, Franco,Libertini, Emanuela,Pagnoni, Ugo M,Parsons, Andrew F
, p. 7925 - 7932 (2007/10/03)
α,β-Unsaturated hydrazones can be easily converted into N-allyl hydrazines by reaction with dimethylamine-borane/p-toluenesulfonic acid under mild reaction conditions. The reduction works well for N′-allylhydrazides but N′-allyl-N,N-dimethylhydrazines are
Studies on quinones. Part 32.1 Regioselective synthesis of benz[b]phenantridines related to phenantroviridone
Valderrama, Jaime A.,Gonzalez, M. Florencia,Valderrama, Claudio
, p. 6039 - 6050 (2007/10/03)
The Diels-Alder reaction of juglone (4) and bromojuglone 18 with 1- cyclohexenecarboxaldehyde dimethylhydrazone (3) is described. Through these cycloaddition reactions 8-hydroxy-1,2,3,4-tetrahydrobenz[b]phenantridin- 7,12-dione (5) was obtained in 55 and
-Cycloadditionen von α,β-ungesaettigten Hydrazonen. Teil 1. Pyridin-2,3-dicarboximide aus 1-(Dimethylamino)-1,4-dihydropyridin-Derivaten
Waldner, Adrian
, p. 486 - 492 (2007/10/02)
Cycloadditions of α,β-Unsaturated Hydrazones to Pyridine-2,3-dicarboximides via 1-(Dimethylamino)-1,4-dihydropyridine Derivatives.The cycloaddition of α,β-unsaturated hydrazones of type 1 (1-aza-1,3-butadienes) with 2-halogenomaleimides 4 affor
