94243-20-6Relevant articles and documents
Reinvestigation of the reaction of 3-substituted 1,2,4-triazines with nitronate anions: unexpected behavior of 3-(2-ethoxyphenyl)-1,2,4-triazine in the reaction with anions of nitroalkanes
Mojzych, Mariusz,Bernat, Zofia,Karczmarzyk, Zbigniew
, p. 968 - 977 (2019)
[Figure not available: see fulltext.] 3-Substituted 1,2,4-triazines easily react with nitronate anions to replace hydrogen atom in the position C-5 according to nucleophilic substitution mechanism and form appropriate oximes of 5-formyl- or 5-acyl-1,2,4-t
Enantioselective reduction of 5-acyl-1,2,4-triazines and their oximes by baker's yeast [1]
Rykowski,Lipinska,Guzik,Adamiuk,Olender
, p. 69 - 76 (2007/10/03)
Variously substituted 5-acyl-1,2,4-triazines 4a-d were regioselectively synthesized through a sequence involving nucleophilic acylation of 1,2,4-triazines 1a-b with nitronate anions 2a-c followed by hydrolysis of the oximes 3a-d thus formed, by sodium hyd