Current position: Home >> Scientific Research >> Paper Publications

1,3-Dipolar Cycloaddition of Azomethine Ylides Involving 3-Aminooxindoles: Versatile Construction of Dispiro[pyrrolidine-2,3 '-oxindole] Scaffolds

Release Time:2019-03-12  Hits:

Indexed by: Journal Article

Date of Publication: 2016-11-01

Journal: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Included Journals: SCIE

Issue: 32

Page Number: 5335-5339

ISSN: 1434-193X

Key Words: Cycloaddition; Diastereoselectivity; Heterocycles; Multicomponent reactions; Spiro compounds

Abstract: A three-component [3+2] cycloaddition involving 3-aminooxindoles, aldehydes, and methyleneindolinone derivatives for the synthesis of dispiro[pyrrolidine-2,3'-oxindole] derivatives was developed. This reaction involves the use of readily available starting materials and mild reaction conditions. It displays broad functional-group tolerance and provides the products in high yields with good to excellent diastereoselectivities.

Prev One:Structural characterization and proton reduction electrocatalysis of thiolate-bridged bimetallic (CoCo and CoFe) complexes

Next One:DFT Studies on Styrene Polymerization Catalyzed by Cationic Rare-Earth-Metal Complexes: Origin of Ligand-Dependent Activities