144752-27-2Relevant academic research and scientific papers
Tetrabutylammonium fluoride promoted lntramolecular Nucleophilic attack of a carbodimide group on an α,β-unsaturated ester group
Molina,Aller,Lorenzo
, p. 283 - 287 (1998)
(N-Aryl, N'-aryl/alkyl) carbodiimides bearing an α,βunsaturated ester moiety in the ortho position undergo cyclization in the presence of tetrabutylammonium fluoride under mild conditions to give dihydroquinazoline derivatives in synthetically useful yields.
Conjugated Heterocumulenes. Synthesis of Conjugated Carbodiimides and their Facile Conversion via Intramolecular Cycloaddition into Nitrogen Heterocycles, Quinoline and Pyridoindole (α-Carboline) Derivatives
Saito, Takao,Ohmori, Hiromasa,Furuno, Eiji,Motoki, Shinichi
, p. 22 - 24 (2007/10/02)
A convenient method is described for the synthesis of conjugated carbodiimides and their application to nitrogen heterocycle synthesis via electrocyclisation-intramolecular Diels-Alder reaction.
