## Abstract A scheme is developed for synthesizing ^14^C labelled α‐acetates of secondary α‐hydroxylated nitrosamines. In this manner ^14^C‐methyl (1‐acetoxy)ethyl nitrosamine and 1‐^14^C‐ethyl (1‐acetoxy)ethyl nitrosamine are synthesized in 16.3 and 33.3% yield, radiochemically pure.
SYNTHESIS OF ETHANOL-1-C 14 , ETHANOL-2-C 14 , ETHYL BROMIDE-1-C 14 , ETHYL BROMIDE-2-C 14 AND C 14 -LABELED METHADONE 1
✍ Scribed by TOLBERT, B. M.; CHRISTENSON, FREDA; CHANG, FRANCES NAI-HSUAN; SAH, PETER P. T.
- Book ID
- 124090171
- Publisher
- American Chemical Society
- Year
- 1949
- Tongue
- English
- Weight
- 275 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0022-3263
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