The ' ' C chemical shifts of triterpenoidal olefins and epoxides related to lanosterol are described and discussed. The epoxide function located in the central part of the tetracyclic steroidal skeleton allows the evaluation of epoxidation-induced shifts (EIS) for several carbons. The most character
The carbon-13 spectra of steroids on the way to ecdysone
β Scribed by William B. Smith
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 347 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
Abstract
A combination of chemical shift reagent effects, partially relaxed spectra, and carbon T~1~ measurements have been used to assign the chemical shifts of the carbons in seven different steroids which have served as intermediates in a synthesis of the steroid moulting hormone ecdysone. The assignments of ergosterol have been completed. It has been shown that the T~1~'s are consistent with the molecular structures.
π SIMILAR VOLUMES
## Abstract Two conflicting assignments have been proposed for the ^13^C NMR signals of 3β²,5β²βcyclic nucleotides. This communication describes selective decoupling experiments for several cyclic nucleotides which provide the correct assignment based on unambiguous experimental evidence.
In the structure elucidation of epoxide-containing natural produck,' we have been confronted with the problem of assignment of configuration of the three-membered ring. Although the relatively high field resonance of epoxide carbons has already been noticed,3 no systematic study has been made on the