Conformational studies of sphingolipids by NMR spectroscopy. II. Sphingomyelin
✍ Scribed by C.Mark Talbott; Igor Vorobyov; Douglas Borchman; K.Grant Taylor; Donald B DuPré; M.Cecilia Yappert
- Book ID
- 117047647
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 353 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.
## Abstract The carbon‐13 spectra of seventeen bicyclo[3.1.1]‐heptane derivatives have been recorded and assigned. Study of the C‐6 and C‐7 chemical shifts permits the conformations to be assigned to the bridged chair, Y‐shaped, or bridged boat conformations. The spectrum of verbenone is anomalous