Cargando…
A facile approach to 2-alkoxyindolin-3-one and its application to the synthesis of N-benzyl matemone
2-Alkoxycarbonylindolin-3-one is synthesized from a methoxyglycine derivative via a 1,2-aza-Brook rearrangement followed by cyclization with bis(trimethylsilyl)aluminum chloride. A short-step synthesis of N-benzyl matemone is successfully carried out using the present indolin-3-one synthesis.
Autores principales: | Shimizu, Makoto, Imazato, Hayao, Mizota, Isao, Zhu, Yusong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064601/ https://www.ncbi.nlm.nih.gov/pubmed/35519860 http://dx.doi.org/10.1039/c9ra02204j |
Ejemplares similares
-
N-Alkylation/aldol reaction of α-aldimino thioesters: a facile three-component coupling reaction
por: Shimizu, Makoto, et al.
Publicado: (2021) -
Double nucleophilic addition to iminomalonate, leading to the synthesis of quaternary α-amino diesters and desymmetrization of the products
por: Shimizu, Makoto, et al.
Publicado: (2019) -
Preparation and facile addition reactions of iminium salts derived from amino ketene silyl acetal and amino silyl enol ether
por: Shimizu, Makoto, et al.
Publicado: (2020) -
2,3-Dimethoxy-2,3-dimethyl-1,4-dioxane as a useful precursor to 2,3-dimethylene-1,4-dioxane for [4+2] cycloaddition reaction
por: Shimizu, Makoto, et al.
Publicado: (2021) -
An umpolung reaction of α-iminothioesters possessing a cyclopropyl group
por: Shimizu, Makoto, et al.
Publicado: (2020)