𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

No coin nor oath required. For personal study only.

✦ 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


ChemInform Abstract: Stereoselective Syn
✍ Guy Solladie; Francoise Colobert; Chakib Kalai 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

## 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

Stereoselective synthesis of conjugated
✍ Guy Solladié; Chakib Kalaï; Marc Adamy; Françoise Colobert 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 174 KB

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.