A biogenetic-type synthesis of (+)-ircinianin (1) via intramolecular Diels-Alder reaction of 2 is described. ..l Ircinianin (l), a sesterterpene isolated from marine sponge Ircinia wistarll , 1s structurally unique among those isolated from the same species such as fasciculatin (3)' and strobilinin
The first synthesis of marine sesterterpene (+)-scalarolide
β Scribed by Xiang-Jian Meng; Yang Liu; Wen-Yuan Fan; Bin Hu; Wenting Du; Wei-Ping Deng
- Book ID
- 104096710
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 332 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The synthesis of the first example of C12 oxygenated marine scalaranic sesterterpenes (+)-scalarolide was achieved through three key steps including the ring-opening rearrangement of epoxide, stereoselective Diels-Alder addition and one-pot c-butenolide formation process, and the absolute configuration of natural scalarolide was confirmed.
π SIMILAR VOLUMES
## 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