Cargando…
Squaramide-Catalyzed Enantioselective Michael Addition of Masked Acyl Cyanides to Substituted Enones
[Image: see text] Masked acyl cyanide (MAC) reagents are shown to be effective umpolung synthons for enantioselective Michael addition to substituted enones. The reactions are catalyzed by chiral squaramides and afford adducts in high yields (90–99%) and with excellent enantioselectivities (85–98%)....
Autores principales: | Yang, Kin S., Nibbs, Antoinette E., Türkmen, Yunus E., Rawal, Viresh H. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2013
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3968543/ https://www.ncbi.nlm.nih.gov/pubmed/24090310 http://dx.doi.org/10.1021/ja409012q |
Ejemplares similares
-
Synthesis of α-Amino Acid Derivatives and Peptides via Enantioselective Addition of Masked Acyl Cyanides to Imines
por: Yang, Kin S., et al.
Publicado: (2014) -
Enantioselective Michael Addition of Cyclic β-Diones to α,β-Unsaturated Enones Catalyzed by Quinine-Based Organocatalysts
por: Wang, Qingqing, et al.
Publicado: (2017) -
Enantioselective direct Michael addition of cyanohydrin ether derivatives to enones catalyzed by chiral bis(guanidino)iminophosphorane organosuperbase
por: Das, Saikat, et al.
Publicado: (2023) -
A bifunctional iminophosphorane squaramide catalyzed enantioselective synthesis of hydroquinazolines via intramolecular aza-Michael reaction to α,β-unsaturated esters
por: Su, Guanglong, et al.
Publicado: (2021) -
Salen Promoted Enantioselective Nazarov Cyclizations
of Activated and Unactivated Dienones
por: Hutson, Gerri E., et al.
Publicado: (2013)