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Stereochemical Assignment of the C21–C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Prediction

✍ Scribed by Yoshihisa Kobayashi; Choon-Hong Tan; Yoshito Kishi

Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
109 KB
Volume
39
Category
Article
ISSN
0044-8249

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✦ Synopsis

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 its diastereomers.

📜 SIMILAR VOLUMES

ChemInform Abstract: Stereochemical Assi
ChemInform Abstract: Stereochemical Assignment of the C21—C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Proof.
✍ Choon-Hong Tan; Yoshihisa Kobayashi; Yoshito Kishi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 25 KB

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