## 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
Syntheses and absolute configurations of the marine sponge purines (+)-agelasimine-A and (+)-agelasimine-B
β Scribed by Masashi Ohba; Kazuaki Iizuka; Hiroyuki Ishibashi; Tozo Fujii
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 664 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0040-4020
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Total Syntheses of (Β±)-Agelasimine-A (VII), (Β±)-Agelasimine-B ( VIII), and (Β±)-Purino-diterpene (XI) and the Structure of Diacetylagelasimine-A (IX). -Central synthetic feature of the total syntheses of (VII) and (VIII), isolated from the marine sponge Agelas mauritiana includes the stereoselective
New 26, 27-cyclosterols, aragusterols E-H, were isolated from the Okinawan marine sponge of the genus Xestospongia. Their structures were determined by spectroscopic measurement and chemical conversion. The absolute configurations of xestokerols A and B were determined by chemical conversion.