36960-12-0Relevant articles and documents
InCl3/Me3SiCl-catalyzed direct michael addition of enol acetates to α,β-unsaturated ketones
Onishi, Yoshiharu,Yoneda, Yuki,Nishimoto, Yoshihiro,Yasuda, Makoto,Baba, Akio
supporting information, p. 5788 - 5791 (2013/01/15)
The direct Michael addition of enol acetates to α,β-unsaturated ketones was achieved using a combination of Lewis acid catalysts, InCl 3 and Me3SiCl, which furnished stable enol-form products that could be further transformed into functionalized 1,5-diketones by reactions with various electrophiles.
