85296-24-8Relevant academic research and scientific papers
STEREOCHEMISTRY OF THE THIYLATION OF 1,2-DINITROALKENES AND 1,4-DINITRO-1,3-DIENES
Mukhina, E. S.,Berkova, G. A.,Pavlova, Z. F.,Lipina, E. S.,Perekalin, V. V.
, p. 1249 - 1254 (2007/10/02)
In thiylation with arenethiolates 1,2-dinitroalkenes form 1-nitro-2-arylthioalkenes in the more stable Z form, and in the absence of a base they form a mixture of the Z and E isomers.During thiylation with arenethiols 1,4-dinitro-1,3-butadienes only give (E,E)-1-nitro-4-arylthio-1,3-dienes.
Conjugated dinitroalkenes in reaction with alkyl and aryl hydrosulfides
Pavlova, Z. F.,Kasem, Ya. A.,Lipina, E. S.,Perekalin, V. V.
, p. 2227 - 2229 (2007/10/02)
Highly electrophilic conjugated 1,2-dinitroalkenes react actively with alkyl and aryl hydrosulfides (ethyl hydrosulfide, thiophenol, p-chlorothiophenol) in the presence of bases to form products from substitution of the nitro group, i.e., nitro(alkyl)aryl
