Stereoselective total syntheses of 9(S)- and 9(R)-HETE
β Scribed by J.S. Yadav; L.R.M. Bhanu; Dinah Dutta
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 476 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
An expedient stereoselective total synthesis of 18-carbon (+)-(6S,9R,10R)-bovidic acid, isolated from the pelage and skin of a gaur B. frontalis is described using L-proline catalysed sequential a-aminoxylation and Horner-Wadsworth-Emmons olefination of aldehyde, cross metathesis and tandem Sharples
A rather facile stereoselective total synthesis of (9S)-9-dihydroerythronolide A starting from D-glucose was achieved via coupling of Cl-C6 and C7-Cl5 segments and subsequent macrolactonizotion. The well known macrolide antibiotic erythromycin A (1) has been an attractive synthetic target for moder