Stereocontrolled synthesis of 5-(1′-hydroxyalkyl)-3-methylidenetetrahydro-2-furanones
✍ Scribed by Tomasz Janecki; Edyta Błaszczyk
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 83 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Diastereo-and enantioselective synthesis of 5-(1%-hydroxyalkyl)-3-methylidenetetrahydro-2-furanones from 2diethoxyphosphoryl-4-alkenoic acids or 2-diethoxyphosphoryl-4-alkenoates was readily accomplished using novel methodology involving syn-or anti-dihydroxylation procedures combined with Horner-Wadsworth-Emmons olefination techniques.
📜 SIMILAR VOLUMES
The reactivity of 5-methyl-4-(pyrrolidin-1-yl)-5H-furan-2-one with aldehydes and with acyl chlorides followed by reduction was studied. The aldol condensation gave predominantly the anti aldol product when the acylation -reduction sequence led exclusively to the syn product. The use of a chiral pyrr
## 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 3,4‐Dichloro‐2(5__H__)‐furanone, which has been prepared efficiently from mucochloric acid, has been transformed selectively into 4‐aryl‐3‐chloro‐2(5__H__)‐furanones either by Suzuki‐ or Stille‐type reactions. These monochloro derivatives have been used as precursors either to (__Z__)‐4