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ChemInform Abstract: Palladium-Catalyzed Reductive Cyclization Reaction in Alkaloid Synthesis - An Enantioselective Total Synthetic Route to (+)- Pumiliotoxin C.

✍ 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

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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

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## 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 β€œFull Text” option. The original article is trackable v