670227-48-2Relevant academic research and scientific papers
An Improved Protocol for the Morita-Baylis-Hillman Reaction Allows Unprecedented Broad Synthetic Scope
Amarante, Giovanni W.,Camilo, Nilton S.,Carpanez, Arthur G.,Coelho, Fernando,Fernandes, Fábio S.,Lima, Samia R.,Rodrigues, Manoel T.,Santos, Hugo,Serafim, José Cláudio,Silva, Thiago S.,Zeoly, Lucas A.,de Oliveira, Aline S. B.
supporting information, (2022/01/22)
The Morita-Baylis-Hillman (MBH) reaction has been stablished as an important C?C bond-forming transformation between carbonyl-containing compounds and activated olefins. However, the slow reaction rate usually observed with electron-rich electrophilic par
Quinolines from Morita-Baylis-Hillman acetates of 2-azidobenzaldehydes
Han, Eun-Gu,Kim, Hea Jung,Lee, Kee-Jung
scheme or table, p. 9616 - 9625 (2010/02/27)
A simple method for synthesizing several 2-alkoxy-3-arylsulfinylmethylquinolines using an aza-Wittig type reaction of 3-(2-azidophenyl)-2-(arylsulfinylmethyl)propenoates, which were readily obtained from the Morita-Baylis-Hillman acetates of 2-azidobenzal
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
