Abstract
The title classes of compounds have been prepared using a sequence of two ring‐forming reactions. Initial 1,3‐dipolar cycloaddition with an azomethine ylide gave N‐acylated 3‐pyrrolines which were further elaborated to the target compounds by a tandem deprotection/cyclization reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 975-979 |
| Number of pages | 5 |
| Journal | Journal of Heterocyclic Chemistry |
| Volume | 27 |
| Issue number | 4 |
| DOIs | |
| State | Published - 1990 |
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Dive into the research topics of 'Synthesis of 3,9b‐dihydro‐5H‐pyrrolo[2,1‐a]isoindoles and 3,5,6,10b‐tetrahydropyrrolo[2,1‐a]isoquinolines with 1,3‐dipolar cycloaddition reactions'. Together they form a unique fingerprint.Cite this
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