Total Synthesis of a Mevinic Acid Analog
β Scribed by Thummalapally Srikanth Reddy; Dorigondla Kumar Reddy; Manchala Narasimhulu; Dasari Ramesh; Yenamandra Venkateswarlu
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- German
- Weight
- 152 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0018-019X
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β¦ Synopsis
Abstract
Total synthesis of mevinic acid analog 1 has been achieved efficiently starting from chiral 2,3βOβisopropylideneβDβglyceraldehyde (2). The synthesis involves Mitsunobu reaction and Evans' intramolecular oxaβMichael synβaddition reactions as key steps.
π SIMILAR VOLUMES
Gangliosides, sialic acid containing glycosphingolipids, are a class of structurally diverse molecules commonly present in vertebrate plasma membranes and especially enriched in nerve tissues\*. These membrane components are thought to be responsible for important physiological activities, and it is