Organocatalytic Enantioselective Synthesis of Oxindole‐4‐Aminopyrazolone Derivatives via Mannich Reaction of 3‐Substituted Oxindoles With Pyrazolinone Ketimines
ABSTRACT The organocatalyzed Mannich reaction between pyrazolinone ketimines and 3‐aryl‐substituted oxindoles mediated by a hidroquinine‐derived squaramide is reported. This method enables the synthesis of a diverse set of oxindole‐4‐aminopyrazolone derivatives bearing vicinal tetrasubstituted stereocenters, affording products in good yields (up to 95%), with excellent diastereoselectivity (> 20:1) and moderate enantioselectivity (up to 85:15 er) under mild conditions.
Authors
- Laura Martín (ORCID: https://orcid.org/0000-0002-6583-8731)
- José M. Andrés (ORCID: https://orcid.org/0000-0002-0595-3789)
- Alicia Maestro (ORCID: https://orcid.org/0000-0003-1941-6981)
- María E. Molinero
- Sandra Tejedor
Institutions
- Universidad de Valladolid (ES)
Publication Details
- Journal
- Journal of Heterocyclic Chemistry
- Published
- 2025-06-30
- DOI
- https://doi.org/10.1002/jhet.70005
- Citations
- 2
- Primary Topic
- Asymmetric Synthesis and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 1.87
Funders
- Universidad de Valladolid
- Junta de Castilla y León