Stereochemical assignment of the C23–C35 portion of sphinxolide/reidispongiolide class of natural products by asymmetric synthesis
✍ Scribed by Angela Zampella; Valentina Sepe; Rosa D'Orsi; Giuseppe Bifulco; Carla Bassarello; Maria Valeria D'Auria
- Book ID
- 104359899
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 466 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0957-4166
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📜 SIMILAR VOLUMES
Stereochemistry can be predicted: The stereoselective synthesis of the C21-C38 degradation product derived from oasomycins A and B has confirmed the stereochemistry predicted from a comparitive study of the NMR chemical shifts of the C21-C38 portion of the natural products with those obtained for it
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