Palladium-Catalyzed Intramolecular Allylic Alkylation Reaction in Marine Natural Product Synthesis. Enantioselective Synthesis of (+)-Methyl Pederate, a Key Intermediate in Syntheses of Mycalamides. -The carbonate precursor (VIII) for the title key step, leading to lactone (IX), is effectively prepa
ChemInform Abstract: A Practical Synthesis of the Key Intermediate for Theopederins — An Enantioselective Total Synthesis of (+)-Methyl Pederate.
✍ Scribed by M. TOYOTA; Y. NISHIKAWA; K. FUKUMOTO
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
An Enantioselective Total Synthesis of (+)-Methyl Pederate. -The key intermediate for theopederins, methyl pederate (IV), is available by a practical route involving the pivotal Pd-catalyzed cyclization of the carbonate (II) as key step. -(TOYOTA, M.;
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## 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 “Full Text” option. The original article is trackable v
## 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 “Full Text” option. The original article is trackable v