Enantioselective Synthesis of Pseudomonic Acids. I. Synthesis of Key Intermediates
✍ Scribed by Bernhard Schönenberger; Walter Summermatter; Camille Ganter
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- German
- Weight
- 219 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
An enantioselective synthesis of key intermediates for the synthesis of the anti‐microbially active pseudomonic acids A (1), B (2) and C (3) is described. D‐Ribose (4) was used as starting material.
📜 SIMILAR VOLUMES
The synthesis of the cis-fused y-lactone 2,7-dioxabicycle-&3,4 non-4-en-g-one (3) by two routes is reported. Its stereoselective conversion to a key intermediate for pseudomonic acid synthesis is described.
The asymmetric synthesis of a template decalin precursor in the synthesis of polyhydroxylated agarofuran sesquiterpenes is described via a Lewis acid catalysed addition of furan to an activated cyclohexenone directed by an adjacent chiral ketal moiety.