Stereocontrolled Total Synthesis of (Β±)-Culmorin via the Intramolecular Double Michael Addition. -The stereocontrolled total synthesis of racemic culmorin (VII) is based on the intramolecular double Michael addition of the cyclopentenone (V) having an Ξ±,Ξ²-unsaturated ester moiety. -
β¦ LIBER β¦
ChemInform Abstract: Intramolecular Addition of Acyldiazenecarboxylates onto Double Bonds in the Synthesis of Heterocycles.
β Scribed by Jose V. Prata; Dina-Telma S. Clemente; Sundaresan Prabhakar; Ana M. Lobo; Isabel Mourato; Paul S. Branco
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 35 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0931-7597
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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 βFull Textβ option. The original article is trackable v
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