## Abstract The ^1^H and ^13^C nmr spectral assignments of [7bR]‐__N__‐[2‐[(4,5,8,8a‐tetrahydro‐7‐methyl‐4‐oxocyclo‐propa[__c__]pyrrolo[3,2‐__e__]indol‐2(1__H__)‐ylcarbonyl]‐1__H__‐indol‐5‐yl]‐2‐benzofurancarboxamide (Adozelesin) (1) are described. Complete and unambiguous assignments of the hydrog
Complete 1H and 13C assignments of fluorinated analogs of dehydroepiandrosterone
✍ Scribed by Jason P. Burgess; James S. Wintermute; Brian F. Thomas; Izet M. Kapetanovic
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 91 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1874
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✦ Synopsis
Abstract
The complete assignments of all ^1^H and ^13^C chemical shifts were made for the fluorinated dehydroepiandrosterone (DHEA) analog fluasterone, 2, and two potential in vivo metabolites 3 and 4. The assignments were made using a combination of one‐ and two‐dimensional NMR techniques (^1^H, ^13^C, gDQCOSY, gHSQC, gHMBC). Once the proton chemical shifts were assigned, the stereochemistry of the two hydroxylated analogs was determined using 2D ROESY experiments. Copyright © 2006 John Wiley & Sons, Ltd.
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