DEIODINATION REACTIONS USING TRIBUTYLTIN HYDRIDE FOR POTENTIAL LABELING EXPERIMENTS
Zippi, EM; Plourde, GW; Satyamurthy, N
| HERO ID | 2302484 |
|---|---|
| In Press | No |
| Year | 1995 |
| Title | DEIODINATION REACTIONS USING TRIBUTYLTIN HYDRIDE FOR POTENTIAL LABELING EXPERIMENTS |
| Authors | Zippi, EM; Plourde, GW; Satyamurthy, N |
| Journal | Journal of Labelled Compounds and Radiopharmaceuticals |
| Volume | 36 |
| Issue | 4 |
| Page Numbers | 361-364 |
| Abstract | 2,6‐Dinitro‐1‐iodobenzene and 2,4‐dinitro‐1‐iodobenzene were deiodinated with tributyltin hydride at different temperatures using various addition modes. The product ratios of 1,3‐dinitrobenzene and the corresponding tributylstannyldinitrobenzene compounds were determined by NMR in order to evaluate the optimum conditions for impending tritiation experiments. Copyright © 1995 John Wiley & Sons, Ltd. |
| Doi | 10.1002/jlcr.2580360408 |
| Wosid | WOS:A1995QR17900009 |
| Is Certified Translation | No |
| Dupe Override | No |
| Comments | Scopus URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028956042&doi=10.1002%2fjlcr.2580360408&partnerID=40&md5=3e1f8ea699bbc9f361e87af689f3c6bb |
| Is Public | Yes |
| Language Text | English |
| Keyword | DEIODINATION; TRIBUTYLTIN HYDRIDE; TRITIATION; ARYLTRIBUTYLTIN |