ChemInform Abstract: Asymmetric Synthesis of Rhopaloic Acid A Analogues and Their Biological Properties.
β Scribed by Hiroko Nishitani; Asami Sasaoka; Munetaka Tokumasu; Katsuo Ohkata
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ Synopsis
Asymmetric Synthesis of Rhopaloic Acid A Analogues and Their Biological Properties.
-In order to study structure-activity relationships of cytotoxic rhopaloic acid, related analogues such as (X) are synthesized. The routes are based on asymmetric alkylation of a chiral oxazolidine (I) and construction of the tetrahydropyran moiety by way of malonic ester synthesis. Compared to rhopaloic acid, the analogues which bear a shorter isoprenoid side chain exhibit decreased activity. -(NISHITANI, HIROKO; SASAOKA,
π SIMILAR VOLUMES
Stereoselective Syntheses of (+)-Rhopaloic Acid A and (-)-ent-and (Β±)-rac-Rhopaloic Acid A. -Total syntheses of natural rhopaloic acid (XIII), its enantiomer and racemate via successive homologation of farnesol (I) and cyclization to form the tetrahydropyran ring are described. The asymmetric synthe
## 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