## Abstract The configurational and conformational relationship at C‐2 and C‐α in the two racemic diastereomeric __endo__‐α‐methyl‐5‐norbornene‐2‐methanols and the corresponding saturated __endo__‐α‐methyl‐2‐norbornanemethanols were determined by first‐order analysis of the ^1^H n.m.r. spectra of t
Analyses of the 500 MHz 1H spectra of the 3-Methyl ethers of estrone, estradiol and their 14α-methyl analogues
✍ Scribed by Karl Bischofberger; James R. Bull; Anthony A. Chalmers
- Book ID
- 102523722
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 390 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
The 500 MHz 'H spectra of the 3-methyl ethers of estrone, estradiol and their 14a-methyl analogues were assigned by proton decoupling and analysed by second-order calculations for chemical shifts and coupling constants. Introduction of a 14a-Me group effects consistent deshielding of 1,3 diaxially disposed protons. Coupling constant values show characteristic changes for ring D protons, and suggest that some minor perturbation in the H-9a, -lla, -1lp region is caused by the additional methyl group.
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