1024043-62-6Relevant academic research and scientific papers
Fe-catalyzed synthesis of substituted N-aryl oxazolidines
Murru, Siva,Lott, Charles Seth,McGough, Brandon,Bernard, Dakota M.,Srivastava, Radhey S.
supporting information, p. 3681 - 3685 (2016/05/09)
A novel iron-catalyzed synthesis of substituted N-aryl oxazolidines was developed via C-N bond formation and methylenation. The reaction of aryl hydroxylamines with allyl alcohols, in the presence of formaldehyde or its equivalents, afforded variety of oxazolidine heterocycles in very good yields. This catalytic method is most effective for para-substituted aryl hydroxylamines and 3-methyl allyl alcohols. Furthermore, acid catalyzed demethylenation of oxazolidines allowed access to N-aryl amino alcohols in good yields.
Behaviour of enaminomalonates and enamidomalonates under various reductive conditions: a novel synthetic approach to N-acetyl-N-aryl β-amino acids
Sol?an, Tomá?,Jakubec, Pavol,Prónayová, Nade?da,Milata, Viktor
, p. 2631 - 2633 (2008/09/19)
The behaviour of enaminomalonates and their deprotection to amines under various reductive conditions is described. A new synthetic approach to N-aryl-N-acetyl-β-amino acids using heterogeneous catalytic hydrogenation has been discovered.
