Two approaches toward the regio- and stereoselective synthesis of N-unsubstituted 3-aryl-4-(trifluoromethyl)-4H-spiro-[chromeno[3,4-c]pyrrolidine-1,3'-oxindoles]

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	679-690
Number of pages	12
Journal	Chemistry of Heterocyclic Compounds
Volume	57
Issue number	6
DOIs	https://doi.org/10.1007/s10593-021-02967-7
Publication status	Published - Jun 2021

1,3-dipolar cycloaddition, 3-nitro-2-(trifluoromethyl)-2H-chromenes, azomethine ylides, benzylamines, cytotoxic activity, isatins, L-phenylglycine, spirochromeno[3,4-c]-pyrrolidines, spiro[pyrrolidine-1,3'-oxindoles], SPIROPYRROLIDINE OXINDOLES, ONE-POT, AZOMETHINE YLIDES, SPIROOXINDOLES, PYRROLIDINE, spiro[pyrrolidine-1,3 '-oxindoles], DIASTEREOSELECTIVE SYNTHESIS, 1,3-DIPOLAR CYCLOADDITION, FACILE, MICROWAVE-ASSISTED SYNTHESIS, DERIVATIVES

ID: 22988713