A New Strategy for the Synthesis of Sphingosine Analogues. Sphingofungin F
β Scribed by Trost, Barry M.; Lee, Chul Bom
- Book ID
- 126854163
- Publisher
- American Chemical Society
- Year
- 1998
- Tongue
- English
- Weight
- 144 KB
- Volume
- 120
- Category
- Article
- ISSN
- 0002-7863
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π SIMILAR VOLUMES
The reaction of the allylic carbonate 2 with organocopper derivatives is the key step of a new strategy for the synthesis of mevinic acid analogues.
A ready asymmetric synthesis of 3Π-oxathionucleosides has overall yield and considerable enantiomeric excesses. It represents a general synthetic path to prepare a wide range been accomplished in three main steps from benzoyloxyethanal. The synthesis is characterized by high of heterosubstituted sul
Ξ±-Lipoic acid / Structural analogues / Tricarbonyl(Ξ· 5 -pentadienyl)iron cations / Carbonyliron complexes / Diimide reduction Dithioester 10 was synthesized in 6 steps from tricarbonyl-also be of interest for the preparation of various labelled compounds and structural analogues. (diene)iron complex