Cargando…
A recyclable stereoauxiliary aminocatalyzed strategy for one-pot synthesis of indolizine-2-carbaldehydes
Indolizine-carbaldehydes with the easily modifiable carbaldehyde group are important synthetic targets as versatile precursors for distinct indolizines. However, the efficient one-pot construction of trisubstituted indolizine-2-carbaldehydes represents a long-standing challenge. Herein, we report an...
Autores principales: | Zeng, Kui, Mei, Ruhuai, Dechert, Sebastian, Ackermann, Lutz, Zhang, Kai |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950359/ https://www.ncbi.nlm.nih.gov/pubmed/36823457 http://dx.doi.org/10.1038/s42004-023-00828-2 |
Ejemplares similares
-
Anomeric Stereoauxiliary Cleavage of the C−N Bond of d‐Glucosamine for the Preparation of Imidazo[1,5‐a]pyridines
por: Zeng, Kui, et al.
Publicado: (2022) -
Novel One-Pot Green Synthesis of Indolizines Biocatalysed by Candida antarctica Lipases
por: Dinica, Rodica Mihaela, et al.
Publicado: (2013) -
Sydnone C-4 heteroarylation with an indolizine ring via Chichibabin indolizine synthesis
por: Albota, Florin, et al.
Publicado: (2016) -
One-Pot Chemoenzymatic Multicomponent Synthesis of Thiazole Derivatives
por: Zheng, Hui, et al.
Publicado: (2013) -
Pot economy and one-pot synthesis
por: Hayashi, Yujiro
Publicado: (2016)