The completely assigned 1H and 13C NMR spectra of the title diastereoisomers in solutions of and CDCl 3 are reported. NOE experiments show that these molecules adopt speciÐc conformations with no rota-DMSO-d 6 tion about the C-2ÈN bond in either solvent. In ring A of the steroid is in a twist-boat c
Vibrational circular dichroism study of [3R,4R]-dideuteriocyclobutane-1,2-dione. Preliminary comparison of experiment and calculations
✍ Scribed by Petr Malon; Timothy A. Keiderling; J.-Y. Uang; James C. Chickos
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 772 KB
- Volume
- 179
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
The preparation, infrared absorption and vibrational circular dicbroism (VCD) spectra of the tide compound are presented.
The absorption intensities and VCD signs and magnitudes were calculated using an ab initio force field and the a priori theory of Stephens, both carried out with a 6-31G** basis set at the SCF level. Excellent agreement was found between theory and experi-, ment for the single-signed VCD seen in the C-H ( t ) and C-D ( -) stretching regions. As predicted, no VCD was detectable in the C-O stretching region. The mid-IR VCD pattern from 1300 to 900 cm-', consisting of two large negative bands and several weak positive bands, was well represented by the calculations.
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