113370-82-4Relevant academic research and scientific papers
A new entry to azomethine ylides from allylic amines and glyoxals: Shifting the reliance on amino ester precursors
Machamer, Natalie K.,Liu, Xiaoxi,Waters, Stephen P.
supporting information, p. 4996 - 4999 (2014/12/11)
The first examples of azomethine ylides derived from allylic amine and glyoxal precursors are reported. The condensation of primary allylic and α-aryl amines with glyoxylates or α-aryl glyoxals affords conjugated azomethine ylides that undergo facile [3 +
X=Y-ZH Systems as Potential 1,3-Dipoles. Part 8. Pyrrolidines and Δ5-Pyrrolines (3,7-Diazabicyclooctenes) from the Reaction of Imines of α-Amino Acids and their Esters with Cyclic Dipolarophiles. Mechanism of Racemisation of α-Amino Acid
Amornraksa, Kitti,Grigg, Ronald,Gunaratne, H. Q. Nimal,Kemp, James,Sridharan, Visuvanathar
, p. 2285 - 2296 (2007/10/02)
Imines of α-amino acid esters with aromatic, heterocyclic, and aliphatic aldehydes generate azomethine ylides stereospecifically by a prototropic shift on heating in toluene.The azomethine ylides undergo cycloaddition to N-phenylmaleimide, maleic anhydrid
