Synthesis of six specifically deuterated analogs of 1,2-dibromo-3-chloropropane
β Scribed by James G. Omichinski; Sidney D. Nelson
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- French
- Weight
- 390 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0022-2135
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The organ-specific toxic potency of subcutaneously administered 1,2-dibromo-3-chloropropane (DBCP) was compared in partially hepatectomized and sham-operated rats over a dose range of 20-80 mg kg-' to assess the roles of hepatic and extrahepatic metabolism in protection against acute renal and gonad
Deuterated methylene groups have been introduced synthetically in selected positions of the sn-2 palmitoyl chain of 1,2-dipalmitoylom-glycero-3-phosphocholine (DPPC) and deuterated methyl groups in the sn-1 and sn-2 palmitoyl chains as well as in the m-3 phosphocholine group. The vibrational spectr