114261-01-7Relevant academic research and scientific papers
THE REACTIVITY OF 1,4-DIHYDRONICOTINAMIDES TOWARDS REDUCTION OF 1,1',1''-TRIFLUOROACETOPHENONE: INFLUENCE OF METHYL SUBSTITUTION ON THE PYRIDINE RING.
Bossaerts, Jan,Dommisse, Roger A.,Alderweireldt, Frank C.
, p. 2235 - 2236 (2007/10/02)
In a series of methyl substituted 1-(2',6'-dichlorobenzyl)-1,4-dihydronicotinamides those compounds with the methyl α to the pyridine nitrogen are at least one order of magnitude more reactive than the analogues without methyl or methyl on the 5-position.
