Cargando…
Knorr-Rabe partial reduction of pyrroles: Application to the synthesis of indolizidine alkaloids
BACKGROUND: The Birch reduction of electron rich pyrroles does not occur readily. However, dissolving metal reduction with zinc under acidic conditions gives 3-pyrrolines (2,5-dihydropyrroles) in reasonable yield. This dissolving metal reduction was first reported by Knorr and Rabe in 1901 but since...
Autores principales: | Gourlay, Brendon S, Ryan, John H, Smith, Jason A |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2238744/ https://www.ncbi.nlm.nih.gov/pubmed/18197983 http://dx.doi.org/10.1186/1860-5397-4-3 |
Ejemplares similares
-
Total synthesis of the indolizidine alkaloid tashiromine
por: Marsden, Stephen P, et al.
Publicado: (2008) -
Synthesis of the Benzo-fused Indolizidine Alkaloid Mimics
por: Comins, Daniel L, et al.
Publicado: (2007) -
Polystyrenesulfonate-catalyzed synthesis of novel pyrroles through Paal-Knorr reaction
por: Banik, Mandira, et al.
Publicado: (2012) -
Synthesis of (–)-Indolizidine 167B based on domino hydroformylation/cyclization reactions
por: Guazzelli, Giuditta, et al.
Publicado: (2008) -
Facile synthesis of two diastereomeric indolizidines corresponding to the postulated structure of alkaloid 5,9E-259B from a Bufonid toad (Melanophryniscus)
por: Nelson, Angela, et al.
Publicado: (2008)