The acetate of (Z)-4-chloro-2-methyl-2-buten-1-ol. Stereoselective wittig synthesis of a new hemiterpenoid synthon
โ Scribed by E. Cereda; M. Attolini; E. Bellora; A. Donetti
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 191 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
a synthetic method for the preparation of the acetate of (Z)-4-chloro-2-methyl-2-butenl-01, a precursor of the (Z)-hydroxy prenyl synthon 1s described
The use of such synthon In the preparation of a metabollte of a prenyl-contalnlng substance 1s also Illustrated
The hemlterpenold group (lsopentenyl, prenyl) present I" various natural substances 132
๐ SIMILAR VOLUMES
## Abstract 3,4โDichloroโ2(5__H__)โfuranone, which has been prepared efficiently from mucochloric acid, has been transformed selectively into 4โarylโ3โchloroโ2(5__H__)โfuranones either by Suzukiโ or Stilleโtype reactions. These monochloro derivatives have been used as precursors either to (__Z__)โ4