An efficient, high specific activity radioiodination of 5-(1-hydroxy/methoxy-2-iodoethyl)-2′-deoxyuridine by isotope exchange labelling in pivalic acid melt-Reference-Cited by-同舟云学术

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An efficient, high specific activity radioiodination of 5-(1-hydroxy/methoxy-2-iodoethyl)-2′-deoxyuridine by isotope exchange labelling in pivalic acid melt

Published:1990-03 Issue:3 Volume:28 Page:247-255
ISSN:0362-4803
Container-title:Journal of Labelled Compounds and Radiopharmaceuticals
language:en
Short-container-title:J Label Compd Radiopharm

Author:

Iwashina Takashi,Kumar Rakesh,Knaus Edward E.,Wiebe Leonard I.

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Radiology Nuclear Medicine and imaging,Biochemistry,Analytical Chemistry

Reference12 articles.

1. Synthesis and tumor uptake of 5-halo-1-(2'-fluoro-2'-deoxy-.beta.-D-ribofuranosyl)[2-14C]uracils

2. Tumor uptake of radiolabeled pyrimidine bases and pyrimidine nucleosides in animal models—I. 6-[3H]-5-fluorouracil

3. Tumor uptake of radiolabeled pyrimidine bases and pyrimidine nucleosides in animal models —II. 6-[3H]-5-fluoro-2′-deoxyuridine

4. Kumar R. Knaus E. E. Wiebe L. I. J. Med. Chem.

5. Tumor localizing agents. IX. Radioiodinated cholesterol

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues;Beilstein Journal of Organic Chemistry;2011-05-26

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