Efficient Phenylsulfenylation and Phenylselenenylation at the 5-Position of Uracil Nucleosides with Disulfide and Diselenide Mediated by [Bis(Trifluoroacetoxy)iodo]Benzene
A series of uracil nucleosides reacted with diphenyl disulfide or diphenyl diselenide in the presence of hypervalent iodine reagent, [bis(trifluoro-acetoxy)iodo]benzene, in acetonitrile to give the corresponding C-5 phenylsulfenylated or phenylselenenylated products respectively in excellent yields.
- Publisher
- Pergamon-Elsevier Science Ltd
- Issue Date
- 1998
- Language
- English
- Article Type
- Article
- Keywords
PROTECTING GROUP; VINYL HALIDES; C-5; IONS; URIDINES; ROUTE
- Citation
HETEROCYCLES, v.48, no.3, pp.437 - 441
- ISSN
- 0385-5414
- Appears in Collection
- Files in This Item
- There are no files associated with this item.
This item is cited by other documents in WoS
| ⊙ Detail Information in WoSⓡ | Click to see |  |
| ⊙ Cited 12 items in WoS | Click to see citing articles in |  |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.