Skip to Main content Skip to Navigation
Journal articles

The Xanthate Route to Lactams

Abstract : Convergent routes to various classes of lactams exploiting the unique radical chemistry of xanthates are described. Emphasis is placed on reactions leading to lactams by direct radical cyclization, by intermolecular additions to alkenes followed by ring closure, and by radical additions to alkenes furnishing amino esters and aminoacids precursors that can be converted into lactams by ionic condensations. The possibility of modifying existing lactam structures is briefly discussed. Four-, five-, six-, seven-and, more rarely, eight-membered lactams can be constructed, including five-, six-, seven-membered lactams fused to aromatic and heteroaromatic rings. The latter are exemplified by oxindoles, azaoxindoles, tetrahydroquinolones, tetrahydroisoquinolones tetrahydroazaquinolones, tetrahydrobenazepinones, and tetrahydropyridoazepinones.
Document type :
Journal articles
Complete list of metadata

https://hal.archives-ouvertes.fr/hal-03416927
Contributor : Samir Zard Connect in order to contact the contributor
Submitted on : Friday, November 5, 2021 - 1:57:00 PM
Last modification on : Tuesday, January 4, 2022 - 6:31:19 AM

File

Lactams-Tetrahedron-Ms-Revised...
Files produced by the author(s)

Identifiers

Collections

Citation

Samir Zard. The Xanthate Route to Lactams. Tetrahedron, Elsevier, 2021, 79, pp.131852. ⟨10.1016/j.tet.2020.131852⟩. ⟨hal-03416927⟩

Share

Metrics

Les métriques sont temporairement indisponibles