Cargando…
Reagent controlled addition of chiral sulfur ylides to chiral aldehydes
The degree of reagent and substrate control in the reaction of chiral sulfur ylides with chiral aldehydes has been investigated. Specifically, the reactions of the two enantiomers of the chiral benzyl sulfonium salt 1 with glyceraldehyde acetonide were studied in detail. Of the two new stereogenic c...
Autores principales: | Aggarwal, Varinder K, Bi, Jie |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2005
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1399452/ https://www.ncbi.nlm.nih.gov/pubmed/16542017 http://dx.doi.org/10.1186/1860-5397-1-4 |
Ejemplares similares
-
Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine Reagents
por: Brown, Michael, et al.
Publicado: (2016) -
α-Photooxygenation of chiral aldehydes with singlet oxygen
por: Walaszek, Dominika J, et al.
Publicado: (2019) -
On the origin of the stereoselectivity in chiral amide-based ammonium ylide-mediated epoxidations
por: Novacek, Johanna, et al.
Publicado: (2016) -
Coronenohelicenes with Dynamic Chirality
por: Weiss, Corinna, et al.
Publicado: (2020) -
Enantioselective nucleophilic difluoromethylation of aromatic aldehydes with Me(3)SiCF(2)SO(2)Ph and PhSO(2)CF(2)H reagents catalyzed by chiral quaternary ammonium salts
por: Ni, Chuanfa, et al.
Publicado: (2008)