ChemInform Abstract: Palladium-Catalyzed Reductive Cyclization Reaction in Alkaloid Synthesis - An Enantioselective Total Synthetic Route to (+)- Pumiliotoxin C.
β Scribed by M. TOYOTA; T. ASOH; K. FUKUMOTO
- Book ID
- 112038681
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Stereoselective Transformation of Enantiopure Cyclohexenol into cis-Hydrindan. An Enantioselective Formal Total Synthetic Route to (+)-Pumiliotoxin C. -Starting from the known chiral acid (I) the biologically interesting title compound (IX) is synthesized. Key step in this approach is the cyclizatio
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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