Cargando…
Reactions of nitroxides XIII: Synthesis of the Morita–Baylis–Hillman adducts bearing a nitroxyl moiety using 4-acryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl as a starting compound, and DABCO and quinuclidine as catalysts
The Morita–Baylis–Hillman adducts bearing a nitroxyl moiety were synthesized from 4-acryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl and aliphatic, aryl and heterocyclic aldehydes.
Autor principal: | Zakrzewski, Jerzy |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458776/ https://www.ncbi.nlm.nih.gov/pubmed/23019486 http://dx.doi.org/10.3762/bjoc.8.171 |
Ejemplares similares
-
Enantioselective, Organocatalytic Morita-Baylis-Hillman and Aza-Morita-Baylis-Hillman Reactions: Stereochemical Issues
por: Mansilla, Javier, et al.
Publicado: (2010) -
Morita–Baylis–Hillman reaction of acrylamide with isatin derivatives
por: Singh, Radhey Mohan, et al.
Publicado: (2014) -
Application of 7-azaisatins in enantioselective Morita–Baylis–Hillman reaction
por: He, Qing, et al.
Publicado: (2016) -
Engineering an Efficient and Enantioselective Enzyme for the Morita-Baylis-Hillman Reaction
por: Crawshaw, Rebecca, et al.
Publicado: (2022) -
Naphthalenes and Quinolines by Domino Reactions of Morita–Baylis–Hillman Acetates
por: Annor-Gyamfi, Joel K., et al.
Publicado: (2020)