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...

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Detalles Bibliográficos
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:
Article
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

Internet

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

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