Conformational studies of sphingolipids by NMR spectroscopy. I. Dihydrosphingomyelin
✍ Scribed by Stacey R Ferguson-Yankey; Douglas Borchman; K.Grant Taylor; Donald B DuPré; M.Cecilia Yappert
- Book ID
- 117047646
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 464 KB
- Volume
- 1467
- Category
- Article
- ISSN
- 0005-2736
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📜 SIMILAR VOLUMES
3 a ) and (3c) or (Sf) formed as minor products on reaction ( I ) with methyl acryiate or methyl propiolate were synthesized isomer-free from the diester (1') and characterized. The data for the compounds prepared are summarized in Table .
## Abstract The ^13^C chemical shift of the substituted or functionalized carbon of various medium and large rings is plotted against ring size (6–15 carbons). The curves thus obtained allow a conformational analysis of the corresponding derivatives.