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Preparation of 77Se-selenomethionine. (S)-(− -¦Á-Amino-¦Ã-butyrolactonehydrochloride (500 mg) was dissolved in HBr-saturated acetic acid (5 mL), followed by refluxing for 5 h. The reaction mixture was allowed to stand for 12 h at room temperature to afford ¦Á-amino-¦Ã-bromobutyric acid hydrobromide as white crystals (yield, 92%). 77Se-Selenium (metal powder, 7.0 mg) wassuspended in dry THF (1 mL) under an atmosphere of nitrogen, and then CH3Li (1 M THF solution, 2.7 mL) was added, followed by stirring at room temperature for 5 min. ¦Á-Amino-¦Ã-bromobutyric acid hydrobromide (71 mg) dissolved in dry ethanol (0.5 mL) was gradually added to the reaction mixture, followed by refluxing for 1 h. The reaction mixture was evaporated in vacuo, and the residue was dissolved in an aqueous solution of HCl (1 M, 1.5 mL) and washed with diethylether (2 mL, twice). The aqueous layer was neutralized with 1 M NaOH and then purified on an ODS column to afford 77Se-SeMet (yield estimated by selenium, 51%). |
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4Â¥2013-03-12 21:45:36
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2Â¥2013-03-12 21:03:56
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obscure nacissus
- Ó¦Öú: 113 (¸ßÖÐÉú)
- ¹ó±ö: 0.299
- ½ð±Ò: 4511.3
- É¢½ð: 579
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- Ìû×Ó: 485
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3Â¥2013-03-12 21:05:34
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- ÔÚÏß: 2433.7Сʱ
- ³æºÅ: 2227382
- ×¢²á: 2013-01-07
- ÐÔ±ð: GG
- רҵ: ÈËÀàÓªÑø
5Â¥2013-03-13 08:03:31













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