Abstract
Convergent routes to a variety of pyrroles involving radical additions of xanthates are described. Emphasis is placed on reactions leading to the formation of 1,4-diketones or 1,4-ketoaldehydes or their synthetic equivalents, which can then be condensed with ammonia or primary amines in a variation of the classical Paal-Knorr synthesis of pyrroles. The modification of pyrroles by direct radical addition is also discussed. 1 Introduction 2 Earlier Routes to Pyrroles 3 The Xanthate Radical Addition-Transfer Process 4 Application to Pyrrole Synthesis 5 Further Variations 6 Direct Modification of Existing Pyrrole Rings 7 Outlook and Perspectives.
| Original language | English |
|---|---|
| Pages (from-to) | 2685-2696 |
| Number of pages | 12 |
| Journal | Synlett |
| Volume | 28 |
| Issue number | 20 |
| DOIs | |
| Publication status | Published - 18 Dec 2017 |
| Externally published | Yes |
Keywords
- 1,4-diketones
- Paal-Knorr reaction
- pyrroles
- radical addition
- xanthates
Fingerprint
Dive into the research topics of 'Convergent Routes to Pyrroles Exploiting the Unusual Radical Chemistry of Xanthates - An Overview'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver