182144-79-2Relevant academic research and scientific papers
Stereoselective organoselenium-induced cyclization of N-allyl acethydrazides to 1,3,4-oxadiazines or N-acetyl pyrazolidines
Tiecco, Marcello,Testaferri, Lorenzo,Marini, Francesca
, p. 11841 - 11848 (1996)
N-Allyl acethydrazides easily give rise to organoselenium-induced cyclization reactions to afford phenylseleno substituted 5,6-dihydro-4H-1,3,4-oxadiazines or N-acetyl pyrazolidines as the kinetically or the thermodynamically controlled products, respectively.
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
