A new method for the mild and selective reduction of aryl nitro groups on solid support
β Scribed by Anitha Hari; Benjamin L. Miller
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 164 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
An efficient method for the solid-phase reduction of aryl nitro groups to anilines is describedβ’ Among the several reagents tried, chromium chloride was found to be most effective for this reaction. For the substrates examined, reduction occurs in high yield regardless of the substitution pattern on the aromatic ring, and without affecting other reducible functionality.
π SIMILAR VOLUMES
We have studied the fluoroalkylation of the glucal 1 and the galactal 4 with dibromodifluoromethane via the 2-C-bromodifluoromethyl-substituted glycosyl bromides 2 and 5, respectively, followed by glycosylation to the methyl Γ-D-gly-