A new route to iodine-labeled N-isopropyl iodoamphetamine via organoboranes
β Scribed by George W. Kabalka; Rajender S. Varma; Yuan-Zhu Gai; Ronald M. Baldwin
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 111 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
N-Isopropyl amphetamineboronic acid was prepared via a new in-situ transmetallation reaction involving sonication. The boronic acid intermediate was radioiodinated via a novel iodination procedure.
π SIMILAR VOLUMES
A novel thia-Fries rearrangement of sulfamates 1 in AlCl 3 giving good yields of para-2 and ortho-3 arylhydroxysulfonamides offers a new and efficient route to these sulfonamides.
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