Methods of molecular mechanics were applied to investigate the conformation of the (methyl 2-O-sulfate-4-methyl-ฮฑ-L-idopyranose) uronic acid (DMIS), in order to correlate the peculiar vicinal proton coupling constants observed in polysaccharides containing the iduronate ring to the conformational ch
A force-field study of alkenyl radical ring closure
โ Scribed by Athelstan L.J. Beckwith; Carl H. Schiesser
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 246 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
In accord with stereoelectronic considerations there is a good correlation between the relative rates, regiochemistry, and stereochemistry of ring closure of w-alkenyl radicals, and the strain energies of transition structures determined by force field calculations. Theoretical studies1 of the ring closure of w-alkenyl radicals have met with only limited success. Thus, MINK)/3 calculations1 give activation energies considerably larger than those obtained experimentally2 and fail to predict the observed degree of preference for zcyclisation of 5-hexenyl and 6-heptenyl radicals.
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