Synthesis and oxidation reactions of a user- and eco-friendly hypervalent iodine reagent
✍ Scribed by Arun P Thottumkara; Thottumkara K Vinod
- Book ID
- 104232258
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 126 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Allylic and benzylic alcohols are cleanly oxidized to the corresponding carbonyl compounds in water or water-THF mixtures using a water-soluble derivative of o-iodoxybenzoic acid. A mechanism involving single electron transfer steps is proposed for this facile and eco-friendly oxidation protocol.
📜 SIMILAR VOLUMES
Oxidation of the 2-methoxyphenols 1c-f with phenyl-Using this method the synthesis of asatone (5a) and its demethoxy analogue (5b) was also accomplished starting iodonium(III) diacetate (PIDA) in methanol resulted in the formation of the cyclohexa-2,4-dienones 4c-f, which dime-from the readily avail
## Abstract Condensation of 3,4‐dimethoxybenzeneethanamine (**3d**) and various benzeneacetic acids, __i.e.__, **4a**–**e**, __via__ a practical and efficient one‐pot __Bischler–Napieralski__ reaction, followed by NaBH~4~ reduction, produced a series of 1‐benzyl‐1,2,3,4‐tetrahydroisoquinolines, __i