Producción CyT
Stobbe Condensation
Artículo
Autoría:
Ajoy K. Banerjee ; Lisbeth Mendoza ; Betzabeth Briceño ; Dioni Arrieche ; Elvia CabreraFecha:
2022Editorial y Lugar de Edición:
Organic and Medicinal Chemistry International JournalRevista:
Stobbe Condensation. Organic Medicinal Chem. Volume 11 Issue 4, vol. 11 (pp. 1-5) - ISSN 2474-7610Organic and Medicinal Chemistry International Journal
ISSN:
2474-7610Resumen *
The Stobbe condensation, a widely used reaction in synthetic organic chemistry, involves the reaction of a diester of succinic acid with a carbonyl compound in the presence of an alkoxide to lead to the formation of alkylidine succinic acids [1]. The formation of an intermediary lactone ester is suggested although rarely observed. The reaction condition, particularly the nature of the metal steers the Stobbe reaction in different directions. The reaction has been widely used for the synthesis of cyclopentanone, cyclohexanone derivatives as well as carbonyl compounds with propionic acid as a side chain. It has also been applied for the synthesis of substituted tetralones, tetrahydronapthalenes, and oestrone derivatives Información suministrada por el agente en SIGEVAPalabras Clave
RISHITINOTETRALONESBENZALDEHYDEDIALKYLSUCCINATE