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Synthesis of (4R*,5S*)-5-acetylamino-4-diethylcarbamoyl-5,6-dihydro-4H-pyran-2-carboxylic acid and its inhibitory action against influenza virus sialidases

✍ Scribed by Sean A Kerrigan; Robin G Pritchard; Paul W Smith; Richard J Stoodley


Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
99 KB
Volume
42
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


Synthesis of (4R*,5R*)-4-acetylamino-5-d
✍ Sean A Kerrigan; Paul W Smith; Richard J Stoodley πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 81 KB

4R\*,5R\*)-4-Acetylamino-5-diethylcarbamoylcyclohex-1-ene-1-carboxylic acid and (3R\*,4R\*)-4-acetylamino-3-diethylcarbamoylcyclohex-1-ene-1-carboxylic acid have been synthesised using a Diels-Alder tactic; both compounds are selective inhibitors of influenza A sialidase, the latter compound being p

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✍ GΓΌnther Ohloff; Wolfgang Giersch; Karl H. Schulte-Elte; Paul Enggist; Edouard De πŸ“‚ Article πŸ“… 1980 πŸ› John Wiley and Sons 🌐 German βš– 467 KB

## Abstract Following a known procedure, a mixture of (βˆ’)‐(2__S__,3__R__)‐ and (+)‐(2__R__,3__R__)‐2,3‐epoxy‐citronellols (**5**) was prepared from (βˆ’)‐(__R__)‐linalool (**3**) __via__ epoxy alcohol **4** and then reduced to (βˆ’)‐(__R__)‐3‐hydroxy‐citronellol (**6**). Sensitized photooxygenation of