## Abstract The conformational preferences of morphine and heroin were studied in gas phase and with inclusion of solvent effects. At 298.15 K, three conformers are significant for isolated morphine, all of them displaying antiperiplanar arrangement for the C2C3OH unit, and there is only one sig
✦ LIBER ✦
DFT conformational study of cysteine in gas phase and aqueous solution
✍ Scribed by A. Fernández-Ramos; E. Cabaleiro-Lago; J.M. Hermida-Ramón; E. Martı́nez-Núñez; A. Peña-Gallego
- Book ID
- 114143811
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 419 KB
- Volume
- 498
- Category
- Article
- ISSN
- 0166-1280
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J a p a n ## Synopsis Poly-S-carboxyniethyl-~cysteine has been prepared by debeiizylation of poly-Srarbobenzoxymethyl-bcysteine with hydrogen bromide in acetic acid. By the infrared spectroscopic method the polymer is found to be in the extended p-conformation with a n antiparallel arrangement of