Electrophillc benzylations of 2,6-dimethylphenol and its ethers give surprisingly hia yields of products of attack at m&a-positions of the aromatic rings.1 Examination of possible mechanisms for meta-benzylation showed that only direct attack at the r&a-positions was consistent with sll the evidence
โฆ LIBER โฆ
Synthesis and allylation at the all O-6 positions of cyclomaltohexaose
โ Scribed by Huang, G.; Wong, K.
- Book ID
- 126585089
- Publisher
- Taylor and Francis Group
- Year
- 2007
- Tongue
- English
- Weight
- 101 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1028-6020
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