- search hit 1 of 1
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 |