## Abstract The ring‐ and side‐chain‐^14^C‐labeled DL‐4,4′‐propylenedi‐2,6‐piperazinediones (I) were synthesized from chloroacetic acid‐1‐^14^C in two steps and from DL‐analine‐1‐^14^C in six steps, respectively. The radiochemical yield for the ring labeling was 24.5%; for the side‐chain labeling i
Tumor localizing agents I. Synthesis and tissue distribution of 14C-labeled and radioiodinated 5,6-diacetoxyindole
✍ Scribed by R. E. Counsell; T. D. Smith; J. Doelle; D. Meier; W. H. Beierwaltes
- Publisher
- John Wiley and Sons
- Year
- 1967
- Tongue
- English
- Weight
- 350 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0022-3549
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