A regio- And stereocontrolled approach to the synthesis of 4-CF3-substituted spiro[chromeno[3,4-C] pyrrolidine-oxindoles] via reversible [3+2] cycloaddition of azomethine ylides generated from isatins and sarcosine to 3-nitro-2-(trifluoromethyl)-2 H -chromenes

A regio- And stereocontrolled approach to the synthesis of 4-CF₃-substituted spiro[chromeno[3,4-C] pyrrolidine-oxindoles] via reversible [3+2] cycloaddition of azomethine ylides generated from isatins and sarcosine to 3-nitro-2-(trifluoromethyl)-2 H -chromenes

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

1,3-DIPOLAR CYCLOADDITION, DIASTEREOSELECTIVE SYNTHESIS, NATURAL-PRODUCTS, CLINICAL-TRIALS, DOPAMINE D-3, SPIROOXINDOLES, HETEROCYCLES, CHEMISTRY, 3-NITRO-2H-CHROMENES, PHARMACEUTICALS

ID: 11445641