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Toward Creation of a Universal NMR Database for Stereochemical Assignment: Complete Structure of the Desertomycin/Oasomycin Class of Natural Products

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

Book ID
120425451
Publisher
American Chemical Society
Year
2001
Tongue
English
Weight
52 KB
Volume
123
Category
Article
ISSN
0002-7863

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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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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v