A novel [4 + 3] annulation between isatin N,N’-cyclic azomethine 1,3-dipole and in situ generated nitrosoalkene for direct preparation of seven-membered heterocyclic spirooxindoles
Author:
Funder
Ministry of Science and Technology of the People's Republic of China
National Key Research and Development Program of China
Publisher
Elsevier BV
Reference25 articles.
1. Construction of turmerone motif-fused spiropyrrolidine oxindoles and their biological evaluation for anticancer activities
2. Diastereomeric Spirooxindoles as Highly Potent and Efficacious MDM2 Inhibitors
3. Highly diastereoselective synthesis of trifluoromethyl containing spiro[pyrrolidin-3,2′-oxindoles] from N-2,2,2-trifluoroethylsubstituted isatin imines and β,γ-unsaturated α-keto esters
4. Organocatalytic Asymmetric Synthesis of Spiro-oxindole Piperidine Derivatives That Reduce Cancer Cell Proliferation by Inhibiting MDM2–p53 Interaction
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