## Abstract A very short and straightforward synthesis towards highly functionalized dienes is described. The homochiral starting material, unsaturated β‐oxo ester 2, can be prepared by enzyme‐catalyzed saponification. The utility of the dienes has been demonstrated in a cycloaddition with __N__‐ph
ChemInform Abstract: Synthesis of Bicyclic Homochiral Dienes by Allylic Rearrangement of Cyclohexenols - Suitable Building Blocks for the Synthesis of Nagilactones.
✍ Scribed by B. WESTERMANN; S. DUBBERKE
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
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 via the “References” option.
📜 SIMILAR VOLUMES
## Abstract α‐Stannylated allylic carbonates (I) smoothly undergo Pd‐catalyzed amination to give the corresponding stannylated allylic amines (III), which are suitable substrates for Pd‐catalyzed Stille coupling reactions [cf.
## 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