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Stereoselective synthesis of all-trans methyl substituted polyenes by reductive elimination and application to the synthesis of all-trans 3-methyl-nona-2,4,6-trienol
✍ Scribed by Guy Solladié; Françoise Colobert; Chakib Kalaı̈
- Book ID
- 104210330
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 117 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The stereoselective synthesis of all-trans 3-methyl-nona-2,4,6-trienol 2 by reductive elimination of the corresponding 1,6-dibenzoate-2-methyl-2(Z),4(Z)-diene is described. This result shows that reductive elimination can be extended to the formation of all-trans methyl substituted polyenes which are present in many natural products biosynthetically made from isoprenic units.
📜 SIMILAR VOLUMES
in this paper is reported the stereoselective synthesis of all-trans-tetraenes by reductive elimination of 1,8-dibenzoate-2,4,6-trienes with sodium amalgam. The method was applied to the syntheses of4E, 6E, BE, 10E-heptatetraene and [~-parinaric acid methyl ester.