The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C
β Scribed by Darren J. Dixon; Steven V. Ley; Dominic J. Reynolds
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 375 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0947-6539
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β¦ Synopsis
The total synthesis of the potential antitumour agent muricatetrocin C has provided an ideal stage for the exploitation and development of new chemistry. A convergent synthetic strategy has been realised incorporating three distinct pieces of methodology, these include a highly diastereoselective hetero-Diels Β± Alder reaction to construct the butenolide terminus, an oxygen to carbon rearrangement to install the trans-2,5-disubstituted tetrahydrofuran ring and a spatial desymmetrisation process to afford the anti-diol unit.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v