670227-56-2Relevant academic research and scientific papers
Using Morita-Baylis-Hillman acetates of 2-azidobenzaldehydes for the synthesis of 2-alkoxy-3-cyanomethylquinolines and alkyl quinoline-3-carboxylates
Kim, Hea Jung,Jeong, Eun Mi,Lee, Kee-Jung
experimental part, p. 965 - 972 (2011/10/04)
Figure represented. A simple method for the synthesis of several 2-alkoxy-3-cyanomethylquinolines and alkyl quinoline-3-carboxylates using iminophosphorane-mediated cyclization reactions of 3-(2-azidophenyl)-2- cyanomethylpropenoates and 3-(2-azidophenyl)-2-nitromethylpropenoates has been developed. These compounds were readily obtained from the Morita-Baylis-Hillman acetates of 2-azidobenzaldehydes using potassium cyanide or sodium nitrite, respectively. J. Heterocyclic Chem., (2011)
Synthesis of 4H-Tetrazolo[1,5-a][1]benzazepines from the Baylis-Hillman Adducts of 2-Azidobenzaldehyde
Lee, Chang Hoon,Song, Young Seok,Cho, Hyun In,Yang, Je Woo,Lee, Kee-Jung
, p. 1103 - 1106 (2007/10/03)
Novel heterocycles, 4H-tetrazolo[1,5-a][1]benzazepines 6 were prepared by the intramolecular 1,3-dipolar cycloaddition reaction of azidophenylcyanomethyl compounds 5. The latter were readily obtained from 2-azidobenzaldehyde through the Baylis-Hillman add
