Tetrahydropyranyl ethers (I) can be efficiently deprotected to furnish the corresponding alcohols (II) using a catalytic amount of stannous chloride in methanol. The reaction conditions are mild enough not to effect multiple bonds, and functional groups such as ester, methoxy or methylenedioxy remai
✦ LIBER ✦
ChemInform Abstract: Selective Deprotection of Tetrahydropyranyl Ethers Catalyzed by β-Cyclodextrin in Water.
✍ Scribed by M. Arjun Reddy; L. Rajender Reddy; N. Bhanumathi; K. Rama Rao
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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