Regio- and diastereoselective lipase-catalyzed preparation of acetylated 2-O-glucosylglycerols
✍ Scribed by Diego Colombo; Fiamma Rondietti; Antonio Scala; Ida M. Taino; Pranca Marinone Albini; Lucio Toma
- Book ID
- 103977067
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 579 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0957-4166
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📜 SIMILAR VOLUMES
The hydroxyl group at C‐5 in racemic 1,2‐__O__‐Cyclohexylidene‐__myo__‐inositol (__rac__‐1) was regio‐ and enantioselectively acylated to give 5‐__O__‐acetyl‐ (2a)‐ or 5‐__O__‐butyryl‐2,3‐__O__‐cyclohexylidene‐__myo__‐inositol (3a), respectively, by treatment of 1 with vinyl acetate or 2,2,2‐trifluo
Prochiral dialkylacetal derivatives of 3-hydroxy-2-hydroxymethylpropanal 6a-e were synthesized from the corresponding 2-substituted diethyl malonates 5a-e and subjected to asymmetric enzymatic acetylation. The diethyl malonates 5a-f were prepared from diethyl chloromethylenemalonate 3 by using eithe