Intramolecular Kulinkovich-de Meijere reactions of various disubstituted alkenes bearing amide groups was written by Madelaine, Claire;Ouhamou, Nouara;Chiaroni, Angele;Vedrenne, Emeline;Grimaud, Laurence;Six, Yvan. And the article was included in Tetrahedron in 2008.Category: benzothiophene This article mentions the following:
A range of amides fitted with (E) or (Z) disubstituted alkene groups were prepared and evaluated in intramol. Kulinkovich-de Meijere reactions. The corresponding aminocyclopropanes, e.g., I, were obtained with high diastereoselectivity. Good yields could be achieved with substrates bearing suitable substitutions at the olefin moieties. In the experiment, the researchers used many compounds, for example, 1,3,2-Dioxathiolane 2,2-dioxide (cas: 1072-53-3Category: benzothiophene).
1,3,2-Dioxathiolane 2,2-dioxide (cas: 1072-53-3) belongs to benzothiophene derivatives. Benzothiophene is a fused ring compound of thiophene ring and benzene ring, which is an important class of heterocycles with advantageous structures. The different substitution patterns in these heterocycles offer new opportunities for drug discovery and other applications in materials science.Category: benzothiophene
Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem