3-Nitro-2H-chromenes in [3+2] cycloaddition reaction with azomethine ylides derived from N-unsubstituted α-amino acids and isatins: regio- and stereoselective synthesis of spirochromeno[3,4-c]pyrrolidines

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

Original language	English
Pages (from-to)	529-540
Number of pages	12
Journal	Chemistry of Heterocyclic Compounds
Volume	55
Issue number	6
DOIs	https://doi.org/10.1007/s10593-019-02490-w
Publication status	Published - 15 Jun 2019

1,3-dipolar cycloaddition, 3-nitro-2H-chromenes, isatins, N-unsubstituted α-amino acids, spirochromeno[3,4-c]pyrrolidines, stabilized azomethine ylides, NATURAL-PRODUCTS, 3-dipolar cycloaddition, DISCOVERY, SPIROOXINDOLES, spirochromeno[3, 1, N-unsubstituted alpha-amino acids, FACILE SYNTHESIS, HETEROCYCLES, 4-c]pyrrolidines, 1,3-DIPOLAR CYCLOADDITION, CONSTRUCTION, 3,3,3-TRIHALOGENO-1-NITROPROPENES SYNTHESIS, MICROWAVE-ASSISTED SYNTHESIS, DERIVATIVES

ID: 10485204