Chroman-4-ones via microwave-promoted domino claisen rearrangement-oxa-michael addition: Synthesis of tabchromones A and B
- Allyl phenyl ethers with a pendant enone substituent undergo, upon microwave irradiation, a domino sequence of Claisen rearrangement and 6-endo-trig-cyclization to furnish functionalized chroman-4-ones. The natural products tabchromones A and B were synthesized via this method.
| Author details: | Bernd SchmidtORCiDGND, Martin Riemer, Uwe SchildeORCiDGND |
|---|---|
| DOI: | https://doi.org/10.1055/s-0034-1379364 |
| ISSN: | 0936-5214 |
| ISSN: | 1437-2096 |
| Title of parent work (English): | Synlett : accounts and rapid communications in synthetic organic chemistry |
| Publisher: | Thieme |
| Place of publishing: | Stuttgart |
| Publication type: | Article |
| Language: | English |
| Year of first publication: | 2014 |
| Publication year: | 2014 |
| Release date: | 2017/03/27 |
| Tag: | Michael addition; Wacker reaction; cyclization; rearrangement; tandem reaction |
| Volume: | 25 |
| Issue: | 20 |
| Number of pages: | 4 |
| First page: | 2943 |
| Last Page: | 2946 |
| Organizational units: | Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie |
| Peer review: | Referiert |
